{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,25]],"date-time":"2023-09-25T20:32:23Z","timestamp":1695673943498},"reference-count":22,"publisher":"Springer Science and Business Media LLC","issue":"18","license":[{"start":{"date-parts":[[1989,9,1]],"date-time":"1989-09-01T00:00:00Z","timestamp":620611200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Klin Wochenschr"],"published-print":{"date-parts":[[1989,9]]},"DOI":"10.1007\/bf01721424","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T10:30:29Z","timestamp":1118572229000},"page":"951-956","source":"Crossref","is-referenced-by-count":1,"title":["Early diagnosis of multiple endocrine neoplasia type IIa"],"prefix":"10.1007","volume":"67","author":[{"given":"H. P. H.","family":"Neumann","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O. A.","family":"M\u00fcller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B. A. J.","family":"Ponder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. G. P.","family":"Mathew","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Telenius","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"W.","family":"Schempp","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Schuemichen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N.","family":"Freudenberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Schollmeyer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF01721424_CR1","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1016\/0165-4608(87)90089-6","volume":"24","author":"MG Butler","year":"1987","unstructured":"Butler MG, Repaske DR, Joseph GM, Phillips JA (1987) High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndrome. Cancer Genet Cytogenet 24:129\u2013135","journal-title":"Cancer Genet Cytogenet"},{"key":"BF01721424_CR2","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1007\/BF00282002","volume":"30","author":"T Caspersson","year":"1970","unstructured":"Caspersson T, Zech L, Johannsson C, Modest EJ (1970) Identification of human chromosomes by DNA-binding fluorescent agents. Chromosoma 30:215\u2013227","journal-title":"Chromosoma"},{"key":"BF01721424_CR3","doi-asserted-by":"crossref","first-page":"1991","DOI":"10.1073\/pnas.81.7.1991","volume":"81","author":"GM Church","year":"1984","unstructured":"Church GM, Gilbert W (1984) Genomic sequencing. PNAS 81:1991\u20131995","journal-title":"PNAS"},{"key":"BF01721424_CR4","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1016\/0165-4608(86)90170-6","volume":"22","author":"AM Duncan","year":"1986","unstructured":"Duncan AM, Greenberg CR (1986) Absence of chromosomal instability in one kindred with multiple endocrine neoplasia type IIa. Cancer Genet Cytogenet 22:109\u2013112","journal-title":"Cancer Genet Cytogenet"},{"key":"BF01721424_CR5","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1016\/0003-2697(84)90381-6","volume":"137","author":"AP Feinberg","year":"1984","unstructured":"Feinberg AP, Vogelstein B (1984) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 137:266\u2013267","journal-title":"Anal Biochem"},{"key":"BF01721424_CR6","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1056\/NEJM198802253180804","volume":"318","author":"RF Gagel","year":"1988","unstructured":"Gagel RF, Tashjian AH, Cummings T, Papathanasopoulos N, Kaplan MM, DeLellis RA, Wolfe HJ, Reichlin S (1988) The clinical outcome of prospective screening for multiple endocrine neoplasia type IIa \u2014 an 18-year experience. N Engl J Med 318:478\u2013484","journal-title":"N Engl J Med"},{"key":"BF01721424_CR7","first-page":"104","volume":"35","author":"HR Haak","year":"1987","unstructured":"Haak HR, Nieuwenhuijzen Kruseman AC (1987) Characteristics of a family with the MEN IIa syndrome. Henry Ford Hosp Med J 35:104\u2013106","journal-title":"Henry Ford Hosp Med J"},{"key":"BF01721424_CR8","first-page":"107","volume":"35","author":"DR Hadden","year":"1987","unstructured":"Hadden DR, O'Reilly F, Kennedy L, Russell C (1987) Multiple endocrine neoplasia type IIa: a Northern Ireland and Australian family. Henry Ford Hosp Med J 35:107\u2013109","journal-title":"Henry Ford Hosp Med J"},{"key":"BF01721424_CR9","volume-title":"published in collaboration with Catogenet Cell Genet","author":"ISCN","year":"1985","unstructured":"ISCN (1985) An international system for human cytogenetic nomenclature. Harnden DG, Klinger HP (eds), published in collaboration with Catogenet Cell Genet (Karger, Basel 1985); also in Birth Defects: Original article series, vol 21, no 1 (March of Dimes Birth Defects Foundation, NY, 1985)"},{"key":"BF01721424_CR10","doi-asserted-by":"crossref","first-page":"561","DOI":"10.7326\/0003-4819-78-4-561","volume":"78","author":"HR Keiser","year":"1973","unstructured":"Keiser HR, Beaven MA, Doppman J, Wells S, Buja LM (1973) Sipple's syndrome: medullary thyroid carcinoma, pheochromocytoma and parathyroid disease. Ann Int Med 78:561\u2013579","journal-title":"Ann Int Med"},{"key":"BF01721424_CR11","doi-asserted-by":"crossref","first-page":"1245","DOI":"10.1073\/pnas.74.3.1245","volume":"74","author":"LM Kunkel","year":"1977","unstructured":"Kunkel LM, Smith KD, Boyer SH, Borgaonkar DS, Wachtel SS, Miller OJ, Breg WR, Jones Jr HW, Rary JM (1977) Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. PNAS 74:1245\u20131249","journal-title":"PNAS"},{"key":"BF01721424_CR12","doi-asserted-by":"crossref","first-page":"1645","DOI":"10.1016\/0042-6989(86)90052-0","volume":"26","author":"GI Liou","year":"1986","unstructured":"Liou GI, Fong S-L, Beattie WG, Cook RG, Leone J, Landers RA, Alvarez RA, Wang C, Li Y, Bridges CDB (1986) Bovine interstitial retinol-binding protein (IRBP) \u2014 isolation and sequence analysis of cDNA clones, characterization and in vitro translation of mRNA. Vision Res 26:1645\u20131654","journal-title":"Vision Res"},{"key":"BF01721424_CR13","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1038\/328527a0","volume":"328","author":"CGP Mathew","year":"1987","unstructured":"Mathew CGP, Chin KS, Easton DF, Thorpe K, Carter C, Liou GI, Fong SL, Bridges CDB, Haak H, Nieuwenhuijzen Kruseman AC, Schifter S, Hansen HH, Telenius H, Telenius-Berg M, Ponder BAJ (1987) A linked genetic marker for multiple endocrine neoplasia type IIa on chromosome 10. Nature 328:527\u2013528","journal-title":"Nature"},{"key":"BF01721424_CR14","doi-asserted-by":"crossref","first-page":"374","DOI":"10.1093\/nar\/16.1.374","volume":"16","author":"Y Nakamura","year":"1988","unstructured":"Nakamura Y, Carlson N, Krapcho K, Gill J, O'Connell P, Leppert M, Lathrop GM, Latonel J-M, White R (1988) Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 (DIOSI5). NAR 16:374","journal-title":"NAR"},{"key":"BF01721424_CR15","volume-title":"Methods in human cytogenetics","author":"RA Pfeiffer","year":"1974","unstructured":"Pfeiffer RA (1974) Cell cultures from blood and bone marrow. In: Schwarzacher HG, Wolf U (eds) Methods in human cytogenetics. Springer Verlag, New York"},{"key":"BF01721424_CR16","doi-asserted-by":"crossref","unstructured":"Ponder BAJ, Ponder MA, Coffey R, Pembrey ME, Gagel RF, Telenius-Berg M, Semple P, Easton DF (1988) Risk estimation and screening in families of patients with medullary thyroid carcinoma. Lancet: 397\u2013400","DOI":"10.1016\/S0140-6736(88)91191-9"},{"key":"BF01721424_CR17","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1007\/BF00291539","volume":"63","author":"W Schempp","year":"1983","unstructured":"Schempp W, Meer B (1983) Cytologic evidence for three human X-chromosomal segments escaping inactivation. Hum Genet 63:171\u2013174","journal-title":"Hum Genet"},{"key":"BF01721424_CR18","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1038\/328528a0","volume":"328","author":"NE Simpson","year":"1987","unstructured":"Simpson NE, Kidd KK, Goodfellow PJ, McDermid H, Myers S, Kidd JR, Jackson CE, Duncan AMV, Farrer LA, Brasch K, Castiglione C, Genel M, Gertner J, Greenberg CR, Gusella JF, Holden JJA, White BN (1987) Assignment of multiple endocrine neoplasia type IIa to chromosome 10 by linkage. Nature 328:528\u2013530","journal-title":"Nature"},{"key":"BF01721424_CR19","doi-asserted-by":"crossref","unstructured":"Sobol H, Salvetti A, Bonnardel C, Lenoir GM (1988) Screening multiple endocrine neoplasia IIa families using DNA markers. Lancet:62","DOI":"10.1016\/S0140-6736(88)91047-1"},{"key":"BF01721424_CR20","doi-asserted-by":"crossref","first-page":"164","DOI":"10.1136\/jmg.21.3.164","volume":"21","author":"S Vandenplas","year":"1984","unstructured":"Vandenplas S, Wiid I, Grobler-Rabie A, Brebner K, Rikkets M, Wallis G, Bester A, Boyd C, Mathew CGP (1984) Blot hybridization analysis of genomic DNA. J Med Genet 21:164\u2013172","journal-title":"J Med Genet"},{"key":"BF01721424_CR21","unstructured":"Van Dyke DL, Jackson CE, Baku VR (1981) Multiple endocrine neoplasia type (MEN 2); an autosomal dominant syndrome with a possible chromosome 20 deletion. Am J Hum Genet 33:69a"},{"key":"BF01721424_CR22","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1136\/jmg.21.2.108","volume":"21","author":"A Zattarale","year":"1984","unstructured":"Zattarale A, Stabile M, Nunziata V, DiGiovanni G, Vecchione R, Ventruto V (1984) Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred. J Med Genet 21:108\u2013111","journal-title":"J Med Genet"}],"container-title":["Klinische Wochenschrift"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01721424.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01721424\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01721424","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,8]],"date-time":"2019-05-08T13:22:19Z","timestamp":1557321739000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01721424"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,9]]},"references-count":22,"journal-issue":{"issue":"18","published-print":{"date-parts":[[1989,9]]}},"alternative-id":["BF01721424"],"URL":"https:\/\/doi.org\/10.1007\/bf01721424","relation":{},"ISSN":["0023-2173","1432-1440"],"issn-type":[{"value":"0023-2173","type":"print"},{"value":"1432-1440","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,9]]}}}