{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,25]],"date-time":"2023-10-25T16:22:03Z","timestamp":1698250923511},"reference-count":21,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1986,6,1]],"date-time":"1986-06-01T00:00:00Z","timestamp":517968000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Neurol"],"published-print":{"date-parts":[[1986,6]]},"DOI":"10.1007\/bf00314426","type":"journal-article","created":{"date-parts":[[2004,10,11]],"date-time":"2004-10-11T00:10:52Z","timestamp":1097453452000},"page":"168-170","source":"Crossref","is-referenced-by-count":9,"title":["Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy"],"prefix":"10.1007","volume":"233","author":[{"given":"G.","family":"Meola","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Scarpini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Velicogna","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Scarlato","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Larizza","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. Fuhrman","family":"Conti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","first-page":"356","volume":"24","author":"BO Berg","year":"1974","unstructured":"Berg BO, Conte F (1974) Duchenne muscular dystrophy in a female with a structurally abnormal X-chromosome. Neurology (Minneap) 24:356","journal-title":"Neurology"},{"key":"CR2","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"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1136\/jmg.20.6.461","volume":"20","author":"BS Emanuel","year":"1983","unstructured":"Emanuel BS, Zackai EH, Tucker SH (1983) Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD. J Med Genet 20:461?463","journal-title":"J Med Genet"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1093\/oxfordjournals.bmb.a071624","volume":"36","author":"AEH Emery","year":"1980","unstructured":"Emery AEH (1980) Duchenne muscular dystrophy: genetic aspects, carrier detection and antenatal diagnosis. Br Med Bull 36:117?122","journal-title":"Br Med Bull"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1136\/jmg.2.1.38","volume":"2","author":"P Ferrier","year":"1965","unstructured":"Ferrier P, Bamatter F, Klein D (1965) Muscular dystrophy (Duchenne) in a girl with Turner's syndrome. J Med Genet 2:38?46","journal-title":"J Med Genet"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1016\/0022-510X(84)90058-3","volume":"64","author":"D Gardner-Medwin","year":"1984","unstructured":"Gardner-Medwin D, Johnston HM (1984) Severe muscular dystrophy in girls. J Neurol Sci 64:79?87","journal-title":"J Neurol Sci"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1212\/WNL.27.6.537","volume":"27","author":"MR Gomez","year":"1977","unstructured":"Gomez MR, Engel AG, Dewald G, Peterson HA (1977) Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins. Neurology (Minneap) 27:537?541","journal-title":"Neurology"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1159\/000131496","volume":"27","author":"RM Greenstein","year":"1980","unstructured":"Greenstein RM, Reardon MP, Chan TS, Middleton AB, Mulivor RA, Greene AE, Coriell LL (1980) An (X;11) translocation in a girl with Duchenne muscular dystrophy. Cytogenet Cell Genet 27:268","journal-title":"Cytogenet Cell Genet"},{"key":"CR9","first-page":"513","volume":"33","author":"PA Jacobs","year":"1981","unstructured":"Jacobs PA, Hunt PA, Mayer M, Bart RD (1981) Duchenne muscular dystrophy (DMD) in a female with an X\/autosome translocation: further evidence that the DMD locus is at Xp21. Am J Hum Genet 33:513?518","journal-title":"Am J Hum Genet"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1136\/jmg.16.5.389","volume":"16","author":"RH Lindenbaum","year":"1979","unstructured":"Lindenbaum RH, Clarke G, Patel C, Moncrieff C, Hughes JT (1979) Muscular dystrophy in an X;1 translocation female suggests that Duchenne locus is on X chromosome short arm. J Med Genet 16:389?392","journal-title":"J Med Genet"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1016\/0022-510X(81)90034-4","volume":"49","author":"G Meola","year":"1981","unstructured":"Meola G, Scarpini E, Silani V, Scarlato G (1981) Manifesting carrier of X-linked Duchenne muscular dystrophy. J Neurol Sci 49:455?463","journal-title":"J Neurol Sci"},{"key":"CR12","first-page":"245","volume":"28","author":"G Meola","year":"1984","unstructured":"Meola G, Scarpini E, Manfredi L, Velicogna M, Pellegrini G, Redi CA, Scarlato G (1984) Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures. Basic Appl Histochem 28:245?255","journal-title":"Basic Appl Histochem"},{"key":"CR13","first-page":"365","volume-title":"Neuromuscular diseases","author":"AF Miranda","year":"1984","unstructured":"Miranda AF, Mongini T (1984) Duchenne muscle culture: current status and future trends. In: Serratrice G, Cros D, Desnuelle C, Gastaut JL, Pelliswer JF, Ponget JP, Schrano A (eds) Neuromuscular diseases. Raven Press, New York, pp 365?371"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1007\/BF00275183","volume":"66","author":"H Moser","year":"1984","unstructured":"Moser H (1984) Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention. Hum Genet 66:17?40","journal-title":"Hum Genet"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"378","DOI":"10.1001\/archneur.1982.00510180056015","volume":"39","author":"BJ Olson","year":"1982","unstructured":"Olson BJ, Fenichel GM (1982) Progressive muscle disease in a young woman with family history of Duchenne's muscular dystrophy. Arch Neurol 39:378?380","journal-title":"Arch Neurol"},{"key":"CR16","first-page":"307","volume":"2","author":"Y Skeate","year":"1969","unstructured":"Skeate Y, Bishop A, Dubowitz V (1969) Differentiation of diseased human muscle in culture. Cell Tissue Kinet 2:307?310","journal-title":"Cell Tissue Kinet"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"720","DOI":"10.1016\/0014-4886(83)90036-5","volume":"79","author":"EJ Thompson","year":"1983","unstructured":"Thompson EJ, Yasin R, Lake BD, Cavanagh NPC (1983) Possible manifestation of the dystrophic X chromosome in muscle cultures from carriers of Duchenne muscular dystrophy. Exp Neurol 79:720?728","journal-title":"Exp Neurol"},{"key":"CR18","first-page":"97","volume":"30","author":"C Verellen","year":"1978","unstructured":"Verellen C, Markovic V, DeMeyer R, Freund M, Laterre C, Worton R (1978) Expression of an X-linked recessive disease in a female due to non-random inactivation of the X chromosome. Am J Hum Genet 30:97 (abstract)","journal-title":"Am J Hum Genet"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1007\/BF00270570","volume":"67","author":"C Verellen-Dumoulin","year":"1984","unstructured":"Verellen-Dumoulin C, Freund M, DeMeyer R, Laterre C, Fr\u00e9d\u00e9ric J, Thompson MW, Markovic VD, Worton RG (1984) Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome. Hum Genet 67:115?119","journal-title":"Hum Genet"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1111\/j.1399-0004.1981.tb01799.x","volume":"20","author":"M Yoshioka","year":"1981","unstructured":"Yoshioka M (1981) Clinically manifesting carriers in Duchenne muscular dystrophy. Clin Genet 20:6?12","journal-title":"Clin Genet"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1136\/jmg.18.6.442","volume":"18","author":"M Zatz","year":"1981","unstructured":"Zatz M, Vianna-Morgante AM, Campos P, Diament AJ (1981) Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. J Med Genet 18:442?447","journal-title":"J Med Genet"}],"container-title":["Journal of Neurology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00314426.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00314426\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00314426","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,3]],"date-time":"2019-04-03T19:08:27Z","timestamp":1554318507000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00314426"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1986,6]]},"references-count":21,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1986,6]]}},"alternative-id":["BF00314426"],"URL":"https:\/\/doi.org\/10.1007\/bf00314426","relation":{},"ISSN":["0340-5354","1432-1459"],"issn-type":[{"value":"0340-5354","type":"print"},{"value":"1432-1459","type":"electronic"}],"subject":[],"published":{"date-parts":[[1986,6]]}}}