{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T02:55:25Z","timestamp":1761101725098},"reference-count":75,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1984,6,1]],"date-time":"1984-06-01T00:00:00Z","timestamp":454896000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1984,6]]},"DOI":"10.1007\/bf00270556","type":"journal-article","created":{"date-parts":[[2004,10,5]],"date-time":"2004-10-05T06:20:37Z","timestamp":1096957237000},"page":"37-47","source":"Crossref","is-referenced-by-count":27,"title":["DNA replication and inactivation patterns in structural abnormality of sex chromosomes"],"prefix":"10.1007","volume":"67","author":[{"given":"Mauricio","family":"Camargo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jaroslav","family":"Cervenka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1002\/ajmg.1320020304","volume":"2","author":"PW Allderdice","year":"1978","unstructured":"Allderdice PW, Miller OJ, Miller DA, Klinger HP (1978) Spreading of inactivation in an (X-14) translocation. Am J Med Genet 2:233?240","journal-title":"Am J Med Genet"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1007\/BF00447286","volume":"33","author":"LI Baranovskaya","year":"1976","unstructured":"Baranovskaya LI, Egolina NA, Zakharov AF, Tsvetkova TG (1976) Isochromosome X in man: Different DNA replication patterns in the long arms. Hum Genet 33:55?60","journal-title":"Hum Genet"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"254","DOI":"10.1136\/jmg.16.4.254","volume":"16","author":"R Bernstein","year":"1979","unstructured":"Bernstein R, Dawson B, Kohl R, Jenkins T (1979) X,15 translocation in a retarded girl: X inactivation pattern and attempt to localize the hexosaminidase A and other loci. J Med Genet 16:254?262","journal-title":"J Med Genet"},{"key":"CR4","first-page":"133","volume":"21","author":"MC Biemont","year":"1978","unstructured":"Biemont MC, Laurent C, Couturier J, Dutrillaux B (1978) Chronologie de la re'plication des bandes des chromosomes secuels dans les lymphocytes de sujets normaux et anormaux. Ann Genet (Paris) 21:133?141","journal-title":"Ann Genet (Paris)"},{"key":"CR5","first-page":"171","volume":"35","author":"E Boyd","year":"1981","unstructured":"Boyd E, Ferguson-Smith MA, Ferguson-Smith ME, Jamieson ME, Russell JE, Aitken DA, Sanger R, Tippett P (1981) A case of X;Y translocation which maps the Xq bands to Xp24?pter (abstract). J Med Genet 35:171","journal-title":"J Med Genet"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1111\/j.1469-1809.1956.tb01390.x","volume":"35","author":"KE Buckton","year":"1971","unstructured":"Buckton KE, Jacobs PA, Rae LA, Newton MS, Sanger R (1971) An inherited X-autosome translocation in man. Ann Hum Genet 35: 171","journal-title":"Ann Hum Genet"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1007\/BF00279048","volume":"54","author":"M Camargo","year":"1980","unstructured":"Camargo M, Cervenka J (1980) Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block. Hum Genet 54:47?53","journal-title":"Hum Genet"},{"key":"CR8","first-page":"757","volume":"34","author":"M Camargo","year":"1982","unstructured":"Camargo M, Cervenka J (1982). Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet 34:757?780","journal-title":"Am J Hum Genet"},{"key":"CR9","first-page":"35","volume":"22","author":"N Canki","year":"1979","unstructured":"Canki N, Dutrillaux B, Tivadar I (1979) Dystrophie musculaire de Duchenne chez une petite fille porteuse d'une translocation t(X;3)(p21;q13) de novo. Ann Genet (Paris) 22:35?39","journal-title":"Ann Genet (Paris)"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00284426","volume":"34","author":"J Cervenka","year":"1976","unstructured":"Cervenka J, Djavadi GR, Gorlin RJ (1976) Partial trisomy 4q syndrome: case report and review. Hum Genet 34:1?9","journal-title":"Hum Genet"},{"key":"CR11","first-page":"583","volume":"24","author":"MM Cohen","year":"1972","unstructured":"Cohen MM, Lin CC, Sybert V, Orecchio EJ (1972) Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet 24:583?597","journal-title":"Am J Hum Genet"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1111\/j.1399-0004.1975.tb01948.x","volume":"8","author":"M Cohen","year":"1975","unstructured":"Cohen M, Rosenman A, Macham-Zadeh S (1975) Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv (2) (p15q21)] in a patient with gonadal dysgenesis. Clin Genet 8:11?17","journal-title":"Clin Genet"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1007\/BF00569351","volume":"49","author":"J Couturier","year":"1979","unstructured":"Couturier J, Dutrillaux B, Pascale G, Odile R, Croquette M-F, Foulinnie JC, Maillard E (1979) Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet 49:364?377","journal-title":"Hum Genet"},{"key":"CR14","first-page":"385","volume":"26","author":"BF Crandall","year":"1974","unstructured":"Crandall BF, Carrell RE, Howard J, Schroeder W, Muller H (1974) Trisomy 13 with a 13-X translocation. Am J Hum Genet 26:385?392","journal-title":"Am J Hum Genet"},{"key":"CR15","first-page":"197","volume":"6","author":"CD Darlington","year":"1953","unstructured":"Darlington CD, Wylie AP (1953) A dicentric cycle in Narcissus. Heredity (Ediniburgh) (Suppl) 6:197?213","journal-title":"Heredity (Ediniburgh)"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1007\/BF02982733","volume":"37","author":"CD Darlington","year":"1939","unstructured":"Darlington CD (1939) Misdivision and the genetics of the centromeres. J Genet 37:341?364","journal-title":"J Genet"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1007\/BF00284761","volume":"41","author":"EF Davidenkova","year":"1978","unstructured":"Davidenkova EF, Verlingskaya DK, Mashkova MV (1978) Structural aberrations of the X chromosome in man. Hum Genet 41:259?279","journal-title":"Hum Genet"},{"key":"CR18","first-page":"277","volume":"54","author":"A Chapelle de la","year":"1966","unstructured":"de la Chapelle A, Wennstr\u00f6m J, Horthing H, Ockey CH (1966) Isochromosome X in man. Part II. Hereditas 54:277?292","journal-title":"Hereditas"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1111\/j.1601-5223.1974.tb01344.x","volume":"76","author":"A Chapelle de la","year":"1974","unstructured":"de la Chapelle A, Stenstrand K (1974) Dicentric human X-chromosomes. Hereditas 76:259?267","journal-title":"Hereditas"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1007\/BF00332115","volume":"52","author":"B Dutrillaux","year":"1975","unstructured":"Dutrillaux B (1975) Traitements dicontinus par la BrdU et coloration par l'acridine orange: obtention de marquages R, Q et intermedias. Chromosoma 52:261?273","journal-title":"Chromosoma"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1111\/j.1399-0004.1982.tb01387.x","volume":"21","author":"Y Ejima","year":"1982","unstructured":"Ejima Y, Sasaki MS, Kaneko A, Tanooka H, Hara Y, Hida T, Konoshita Y (1982) Possible inactivation of part of chromosome 13 due to 13qXp translocation, associated with retinoblastoma. Clin Genet 21:357?361","journal-title":"Clin Genet"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1159\/000130131","volume":"10","author":"W Engel","year":"1971","unstructured":"Engel W, Vogel W, Reinwein H (1971)Autoradiographische Untersuchungen an einer X-autosomen Translokation beim Menschen: 45,X,15-,tan(15qXq+)+. Cytogenetics 10:87?98","journal-title":"Cytogenetics"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1159\/000130367","volume":"14","author":"M Fellows","year":"1975","unstructured":"Fellows M, Pearson PL, van der Linden AGJM, Meerakhan P, Hagemeijer A (1975) Mapping the Xqa red blood cell antigen in human-Chinse hamster cell hybrids: the Xq locus is possibly located on the short arm of the X chromosome. Cytogenet Cell Genet 14: 293?295","journal-title":"Cytogenet Cell Genet"},{"key":"CR24","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1007\/BF00295421","volume":"39","author":"M Fraccaro","year":"1977","unstructured":"Fraccaro M, Maraschio P, Pasquali F, Scappaticci S (1977) Women heterozygous for deficiency of the (q21?pter) region of the X-chromosome are fertile. Hum Genet 39:283?291","journal-title":"Hum Genet"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1007\/BF00287006","volume":"39","author":"H Fujita","year":"1977","unstructured":"Fujita H, Tanigawa Y, Yoshida Y, Okada Y (1977) Cytological findings of ten cases with i(Xq) and one with dic(X)(qter?cen?p22::p11?qter). Hum Genet 39:147?155","journal-title":"Hum Genet"},{"key":"CR26","doi-asserted-by":"crossref","first-page":"396","DOI":"10.1159\/000152900","volume":"27","author":"M Gaal","year":"1977","unstructured":"Gaal M, Laszlo J (1977), X inactivation pattern in an unbalaniced X-autosome translocation with gonadal dysgenesis. Hum Hered 27: 396?402","journal-title":"Hum Hered"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1093\/oxfordjournals.jhered.a108794","volume":"68","author":"JE Garcia","year":"1977","unstructured":"Garcia JE, Cummings DK, Wentz AC, Jones HW Jr, Rary JM (1977) A 5\/X chromosomal translocation in a patient with premature menopause. J Hered 68:75?80","journal-title":"J Hered"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1007\/BF00328535","volume":"66","author":"K Goto","year":"1978","unstructured":"Goto K, Maeda S, Kano Y, Sugiyama T (1978) Factors involved in differential Giemsa-staining of sister chromatids. Chromosoma 66: 351?359","journal-title":"Chromosoma"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1159\/000130780","volume":"18","author":"A Hagemeijer","year":"1977","unstructured":"Hagemeijer A, Hoovers J, Smith EME, Bootsma D (1977) Replication pattern of the X chromosome in three X-autosomal translocations. Cytogenet Cell Genet 18:333?348","journal-title":"Cytogenet Cell Genet"},{"key":"CR30","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1007\/BF00569697","volume":"60","author":"B Hellkuhl","year":"1982","unstructured":"Hellkuhl B, de la Chapelle A, Crezeschik KH (1982) Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X-autosome translocation. Hum Genet 60:126?129","journal-title":"Hum Genet"},{"key":"CR31","doi-asserted-by":"crossref","first-page":"496","DOI":"10.1136\/jmg.13.6.496","volume":"13","author":"RT Howell","year":"1976","unstructured":"Howell RT, Roberts SH, Beard RJ (1976) Dicentric X isochromosome in man. J Med Genet 13:496?500","journal-title":"J Med Genet"},{"key":"CR32","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1136\/jmg.15.3.222","volume":"15","author":"LYF Hsu","year":"1978","unstructured":"Hsu LYF, Paciuc S, David K, Cristian S, Moloshok R, Hirschhorn K (1978) Number of C-bands of human isochromosomes Xqi and relation to 45,X mosaicism. J Med Genet 15:222?226","journal-title":"J Med Genet"},{"key":"CR33","first-page":"1","volume":"32","author":"Human Gene Mapping 6","year":"1981","unstructured":"Human Gene Mapping 6 (1981) Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet 32, Nos. 1?4","journal-title":"Cytogenet Cell Genet"},{"key":"CR34","first-page":"736","volume":"26","author":"MB Jenkins","year":"1974","unstructured":"Jenkins MB, Davis E, Thelen TH, Boyd L (1974) A familial X-22 translocation with an extra X chromosome. Am J Hum Genet 26:736?745","journal-title":"Am J Hum Genet"},{"key":"CR35","doi-asserted-by":"crossref","first-page":"3395","DOI":"10.1073\/pnas.70.12.3395","volume":"70","author":"SA Latt","year":"1973","unstructured":"Latt SA (1973) Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. Proc natl Acad Sci USA 70:3395?3399","journal-title":"Proc natl Acad Sci USA"},{"key":"CR36","doi-asserted-by":"crossref","first-page":"412","DOI":"10.1016\/0014-4827(74)90733-2","volume":"86","author":"SA Latt","year":"1974","unstructured":"Latt SA (1974) Microfluorometric analysis of DNA replication in human X chromosomes. Exp Cell Res 86:412?415","journal-title":"Exp Cell Res"},{"key":"CR37","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1007\/BF01538452","volume":"1","author":"SA Latt","year":"1975","unstructured":"Latt SA (1975) Fluorescence, analysis of late DNA replication in human metaphase chromosomes. Somatic Cell Genet 1:293?321","journal-title":"Somatic Cell Genet"},{"key":"CR38","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1007\/BF00292912","volume":"57","author":"SA Latt","year":"1976","unstructured":"Latt SA, Willard HF, Gerald PS (1976) BrudU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes. chromosoma 57:135?153","journal-title":"chromosoma"},{"key":"CR39","first-page":"35","volume":"26","author":"C Laurent","year":"1975","unstructured":"Laurent C, Biemont MC, Dutrillaux B (1975) Sur quatre nouveaux cas de translocations du chromosome X chez l'homme. Humangenetik 26:35?46","journal-title":"Humangenetik"},{"key":"CR40","first-page":"441","volume":"27","author":"JT Leisti","year":"1975","unstructured":"Leisti JT, Kaback MM, Rimoin DL (1975) Human X-autosome translocation: differential inactivation of the X chromosome in a kindred with an X-9 translocation. Am J Hum Genet 27:441?453","journal-title":"Am J Hum Genet"},{"key":"CR41","first-page":"901","volume":"18","author":"MV Mashkova","year":"1976","unstructured":"Mashkova MV, Verlinskaya DK (1976) Familial X-autosome, translocation: t(X,2). Tsitologiia 18:901?905","journal-title":"Tsitologiia"},{"key":"CR42","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1007\/BF00284758","volume":"41","author":"MG Mattei","year":"1978","unstructured":"Mattei MG, Mattei JF, Ayme S, Malpuech G Giraud F (1978) A dynamic study in two new cases of X-chromosome translocations. Hum Genet 41:251?258","journal-title":"Hum Genet"},{"key":"CR43","doi-asserted-by":"crossref","first-page":"401","DOI":"10.1007\/BF00274702","volume":"56","author":"MG Mattei","year":"1981","unstructured":"Mattei MG, Mattei JF, Vidal I, Giraud F (1981) Structural anomalies of the X chromosome and inactivation center. Hum Genet 56: 401?408","journal-title":"Hum Genet"},{"key":"CR44","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1007\/BF00276593","volume":"61","author":"MG Mattei","year":"1982","unstructured":"Mattei MG, Mattei JF, Ayme S, Giraud F (1982) X-autosome translocations: Cytogenetic characteristics and their consequences. Hum Genet 61:295?309","journal-title":"Hum Genet"},{"key":"CR45","doi-asserted-by":"crossref","first-page":"5779","DOI":"10.1073\/pnas.76.11.5779","volume":"76","author":"T Mohandas","year":"1979","unstructured":"Mohandas T, Shapiro LJ, Sparkes RS, Sparkes MC (1979) Regional assignment of the steroid sulfatase-X-linked ichthyosis locus: Implications for a nonactivated region on the short arm of the human X-chromosome. Proc Natl Acad Sci USA 76:5779?5783","journal-title":"Proc Natl Acad Sci USA"},{"key":"CR46","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1159\/000131572","volume":"29","author":"T Mohandas","year":"1981","unstructured":"Mohandas T, Crandall BF, Sparkes RS, Passage MB, Sparkes MC (1981) Late replication studies in a human X\/13 translocation correlation with autosomal gene expression. Cytogenet Cell Genet 29:215?220","journal-title":"Cytogenet Cell Genet"},{"key":"CR47","first-page":"811","volume":"34","author":"T Mohandas","year":"1982","unstructured":"Mohandas T, Sparkes RS, Shapiro LJ (1982) Genetic evidence for the inactivation of a human autosomal locus attached to an inactive X chromosome. Am J Hum Genet 34:811?817","journal-title":"Am J Hum Genet"},{"key":"CR48","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1007\/BF00278972","volume":"54","author":"CR M\u00fcller","year":"1980","unstructured":"M\u00fcller CR, Westerveld A, Migl B, Franke W, Ropers HH (1980) Regional assignment of the gene locus for steroid sulfatase. Hum Genet 54:201?204","journal-title":"Hum Genet"},{"key":"CR49","doi-asserted-by":"crossref","first-page":"621","DOI":"10.1016\/0002-9394(80)90276-7","volume":"89","author":"WW Nichols","year":"1980","unstructured":"Nichols WW, Miller RC, Sobel M, Hoffman E, Sparkes RS, Mohandas T, Veomett I, Davis JR (1980) Further observations on a 13qXp translocation associated with retinoblastoma. Am J Ophthalmol 89:621?627","journal-title":"Am J Ophthalmol"},{"key":"CR50","first-page":"90","volume":"15","author":"E Niebuhr","year":"1982","unstructured":"Niebuhr E (1982) Unusual findings by fluorescence microscopy of a t(13q14q). Humangenetik 15:90?92","journal-title":"Humangenetik"},{"key":"CR51","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1111\/j.1601-5223.1977.tb01220.x","volume":"86","author":"E Niebuhr","year":"1977","unstructured":"Niebuhr E, Skovby F (1977) Cytogenetic studies in seven individuals with an i(Xq) karyotype. Hereditas 86:121?128","journal-title":"Hereditas"},{"key":"CR52","first-page":"1","volume":"3","author":"J Nusbacher","year":"1968","unstructured":"Nusbacher J, Hirschhorn K (1968) Autosomal anomalies in man. Adv Teratol 3:1?63","journal-title":"Adv Teratol"},{"key":"CR53","first-page":"159","volume":"57","author":"PG Otto","year":"1981","unstructured":"Otto PG, Vianna-Morgante AM, Otto PM, Wajutal A (1981) The Turner phenotype and the different types of human X isochromosomes. Hum Genet 57:159?164","journal-title":"Hum Genet"},{"key":"CR54","first-page":"179","volume":"32","author":"CG Palmer","year":"1980","unstructured":"Palmer CG, Hubbard TW, Henry GW, Weaver DD (1980) Failure of X inactivation in the autosomal segment of an X\/autosome translocation. Am J Hum Genet 32:179?187","journal-title":"Am J Hum Genet"},{"key":"CR55","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1038\/251156a0","volume":"251","author":"P Perry","year":"1974","unstructured":"Perry P, Wolff S (1974) New Giemsa method for the differential staining of sister chromatids. Nature 251:156?158","journal-title":"Nature"},{"key":"CR56","first-page":"158","volume":"22","author":"G Pescia","year":"1979","unstructured":"Pescia G, Jotterand-Belloma M, de Crousaz H, Payot M Martin D (1979) Phenotype de la trisomie 9q distale chez un enfant presentant un chromosome surnumeraire remanie [t(X;9)]. Ann Genet (Paris) 22:158?162","journal-title":"Ann Genet (Paris)"},{"key":"CR57","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1007\/BF00303003","volume":"60","author":"PE Polani","year":"1982","unstructured":"Polani PE (1982) Pairing of X and Y chromosomes, noniactivation of X-linked genes and the maleness factor. Hum Genet 60:207?211","journal-title":"Hum Genet"},{"key":"CR58","doi-asserted-by":"crossref","first-page":"378","DOI":"10.1136\/jmg.12.4.378","volume":"12","author":"JH Priest","year":"1975","unstructured":"Priest JH, Blackstone RD, Au KS, Ray LS (1975) Differences in human X isochromosomes. J Med Genet 12:378?389","journal-title":"J Med Genet"},{"key":"CR59","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1007\/BF00276602","volume":"61","author":"HH Ropers","year":"1982","unstructured":"Ropers HH, Zuffardi O, Bianchi E, Tiepolo L (1982) A genesis of corpus callosum, ocular and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X\/3 translocation. Hum Genet 61:364?368","journal-title":"Hum Genet"},{"key":"CR60","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1111\/j.1399-0004.1980.tb00155.x","volume":"17","author":"ME Sands","year":"1980","unstructured":"Sands ME (1980) Mental retardation in association with a balanced X-autosome translocation and random inactivation of the X chromosomes. Clin Genet 17:309?316","journal-title":"Clin Genet"},{"key":"CR61","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1093\/genetics\/37.2.125","volume":"37","author":"ER Sears","year":"1952","unstructured":"Sears ER, Camara A (1952) A transmissible dicentric chromosome. Genetics 37:125?135","journal-title":"Genetics"},{"key":"CR62","doi-asserted-by":"crossref","first-page":"1224","DOI":"10.1126\/science.156396","volume":"204","author":"LJ Shapiro","year":"1979","unstructured":"Shapiro LJ, Mohandas T, Weiss R, Romeo G (1979) Noninactivation of an X chromosome locus in man. Science 204:1224?1226","journal-title":"Science"},{"key":"CR63","first-page":"365","volume-title":"Genetic mechanisms of sexual development","author":"JL Simpson","year":"1979","unstructured":"Simpson JL (1979) Gonadal dysgenesis and sex chromosome abnormalities: phenotypic-karyotypic correlation. In: Vallet HL, Porter IH (eds) Genetic mechanisms of sexual development. Academic Press, New York, pp 365?405"},{"key":"CR64","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1016\/S0022-3476(74)80674-8","volume":"84","author":"RL Summitt","year":"1974","unstructured":"Summitt RL, Martens PR, Wilroy RS (1974) X-autosome translocation in normal father and effectivety 21-monosomic daughter. J Pediatr 84:539?546","journal-title":"J Pediatr"},{"key":"CR65","first-page":"410","volume":"23","author":"TH Thelen","year":"1971","unstructured":"Thelen TH, Abrams DJ, Fisch RO (1971) Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation. Am J Hum Genet 23:410?418","journal-title":"Am J Hum Genet"},{"key":"CR66","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00281002","volume":"25","author":"E Therman","year":"1974","unstructured":"Therman E, Patau K (1974) Abnormal X chromosomes in man: Origin, behavior and effects. Humangenetik 25:1?16","journal-title":"Humangenetik"},{"key":"CR67","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1007\/BF00328482","volume":"59","author":"E Therman","year":"1976","unstructured":"Therman E, Sarto GE, Disteche C, Denniston C (1976) A possible active segment on the inactive human X-chromosome. Chromosoma 59:137?145","journal-title":"Chromosoma"},{"key":"CR68","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1007\/BF00295590","volume":"50","author":"E Therman","year":"1979","unstructured":"Therman E, Sarto GE, Palmer CG, Kallio H Denniston C (1979) Postion of the human X inactivation center on Xq. Hum Genet 50: 59?64","journal-title":"Hum Genet"},{"key":"CR69","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1007\/BF00278961","volume":"54","author":"E Therman","year":"1980","unstructured":"Therman E, Denniston C, Sarto GE, Ulber M (1980) X chromosome constitution and the human female phenotype. Hum Genet 54: 133?143","journal-title":"Hum Genet"},{"key":"CR70","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1007\/BF00278973","volume":"54","author":"L Tiepolo","year":"1980","unstructured":"Tiepolo L, Zuffardi O, Fraccaro M, diNatale D, Gargantini L, Muller CR, Ropers HH (1980) Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. Hum Genet 54:205?206","journal-title":"Hum Genet"},{"key":"CR71","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1007\/BF00293779","volume":"37","author":"C Turleau","year":"1977","unstructured":"Turleau C, Chayin-Colin F, deGrouchy J, Repesse G, Beauvais P (1977) Familial t(X;22)(p223;q323) with partial trisomy 2q and male and female carriers. Hum Genet 37:97?104","journal-title":"Hum Genet"},{"key":"CR72","doi-asserted-by":"crossref","first-page":"1268","DOI":"10.1126\/science.1257746","volume":"191","author":"JJ Yunis","year":"1976","unstructured":"Yunis JJ (1976) High resolution of human chromosomes. Science 191:1268?1270","journal-title":"Science"},{"key":"CR73","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1002\/ajmg.1320010307","volume":"1","author":"BU Zabel","year":"1978","unstructured":"Zabel BU, Baumann WA, Pirntke W, Gerhard-Ratschau K (1978) X inactivation pattern in three cases of X-autosome translocation. Am J Med Genet 1:309","journal-title":"Am J Med Genet"},{"key":"CR74","first-page":"327","volume":"95","author":"AF Zakharov","year":"1976","unstructured":"Zakharov AF, Egolina NA (1976) Correlation between patterns of DNA replication and chromosome banding. Biol Zbl 95:327?334","journal-title":"Biol Zbl"},{"key":"CR75","first-page":"191","volume":"20","author":"O Zuffardi","year":"1977","unstructured":"Zuffardi O, Tiepolo L, Scappaticci S, Francesconi D, Bianchi C, Pinatole D (1977) Reduced phenotypic effect of partial trisomy 1q in a X\/1 translocation. Ann Genet (Paris) 20:191?194","journal-title":"Ann Genet (Paris)"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00270556.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00270556\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00270556","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,29]],"date-time":"2023-04-29T12:46:25Z","timestamp":1682772385000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00270556"}},"subtitle":["I. X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics"],"short-title":[],"issued":{"date-parts":[[1984,6]]},"references-count":75,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1984,6]]}},"alternative-id":["BF00270556"],"URL":"https:\/\/doi.org\/10.1007\/bf00270556","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,6]]}}}