{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T05:10:08Z","timestamp":1760764208187,"version":"build-2065373602"},"reference-count":9,"publisher":"BMJ","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1989,3]]},"abstract":"<jats:p>This paper reports two second cousins with absence of the left hand.<\/jats:p>","DOI":"10.1136\/jmg.26.3.190","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:11:11Z","timestamp":1226329871000},"page":"190-192","source":"Crossref","is-referenced-by-count":4,"title":["Unilateral absence of the hand in second cousins."],"prefix":"10.1136","volume":"26","author":[{"given":"M","family":"Lamont","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A J","family":"Salisbury","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1989,3,1]]},"reference":[{"key":"ref_1","article-title":"Congenital deformities of the upper extremities","author":"Birch-Jensen, A.","year":"1949","unstructured":"Birch-Jensen A. Congenital deformities of the upper extremities. Copenhagen: Munksgaard, 1949."},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1111\/j.1399-0004.1981.tb01834.x","article-title":"Recurrent unilateral hand malformation in siblings","volume":"20","author":"Hecht, J.T.; CL, Jr, Scott","year":"1981","unstructured":"Hecht JT, Scott CL Jr. Recurrent unilateral hand malformation in siblings. Clin Genet 1981;20:225-8.","journal-title":"Clin Genet"},{"key":"ref_3","first-page":"274","article-title":"Hand-reduction malformations: genetic and syndromic analysis","volume":"5","author":"Pilarski, R.T.; Pauli, R.M.; Eligber, W.D.","year":"1985","unstructured":"Pilarski RT, Pauli RM, Eligber WD. Hand-reduction malformations: genetic and syndromic analysis. 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Dominant ectrodactyly and possible germinal mosaicism. J Med Genet 1972;9:318-20.","journal-title":"J Med Genet"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"496","DOI":"10.1038\/315496a0","article-title":"Differential activity of maternally and paternally derived chromosome regions in mice","volume":"315","author":"Cattanach, B.M.; Kirk, M.","year":"1985","unstructured":"Cattanach BM, Kirk M. Differential activity of maternally and paternally derived chromosome regions in mice. Nature 1985; 315:496-8.","journal-title":"Nature"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1038\/328251a0","article-title":"Degree of methylation of transgenes is dependent on gamete of origin","volume":"328","author":"Sapienza, C.; Peterson, A.C.; Rossant, J.; Balling, R.","year":"1987","unstructured":"Sapienza C, Peterson AC, Rossant J, Balling R. Degree of methylation of transgenes is dependent on gamete of origin. Nature 1987;328:251-4.","journal-title":"Nature"},{"key":"ref_9","unstructured":"Case report The proband, a 13 year old mentally retarded male, was referred because of poor secondary sexual development and gynaecomastia. He was thought to be a possible case of Prader-Willi syndrome. He was born at 37 weeks' gestation weighing 1956 g to healthy and unrelated parents. Two sibs, one younger and one older, are both healthy and normal. At two years, the patient's right testis was brought down surgically and the other descended spontaneously at seven years. His development has","article-title":"Case report The proband, a 13 year old mentally retarded male, was referred because of poor secondary sexual development and gynaecomastia. He was thought to be a possible case of Prader-Willi syndrome. He was born at 37 weeks' gestation weighing 1956 g to healthy and unrelated parents. Two sibs, one younger and one older, are both healthy and normal. At two years, the patient's right testis was brought down surgically and the other descended spontaneously at seven years. His development has"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.26.3.190","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T04:52:48Z","timestamp":1760763168000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.26.3.190"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,3]]},"references-count":9,"journal-issue":{"issue":"3","published-online":{"date-parts":[[1989,3,1]]},"published-print":{"date-parts":[[1989,3]]}},"alternative-id":["10.1136\/jmg.26.3.190"],"URL":"https:\/\/doi.org\/10.1136\/jmg.26.3.190","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"type":"print","value":"0022-2593"},{"type":"electronic","value":"1468-6244"}],"subject":[],"published":{"date-parts":[[1989,3]]}}}