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The mode of inheritance of this lethal genetic syndrome is probably autosomal recessive.<\/jats:p>","DOI":"10.1136\/jmg.17.2.119","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"119-122","source":"Crossref","is-referenced-by-count":79,"title":["Syndrome of polydactyly, cleft lip\/palate or lingual lump, and psychomotor retardation in endogamic gypsies."],"prefix":"10.1136","volume":"17","author":[{"given":"V","family":"V\u00e1radi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L","family":"Szab\u00f3","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Z","family":"Papp","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1980,4,1]]},"reference":[{"issue":"1","key":"ref_1","first-page":"790","article-title":"Multiple congenital anomaly caused by an extra autosome","volume":"1960","author":"Patau, K.; Smith, D.W.; Therman, E.; Inhorn, S.L.; Wagner, H.P.","unstructured":"Patau K, Smith DW, Therman E, Inhorn SL, Wagner HP. 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Paris: Expansion Scientifique Francaise, 1977."},{"key":"ref_4","first-page":"342","article-title":"Hochgradiger Mikrophthalmus beim Patau-Syndrom","volume":"173","author":"Pap, Z.; Buczk6, I.; Sz, Szakill; Papp, Z.","year":"1978","unstructured":"Pap Z, Buczk6 I, Szakill Sz, Papp Z. Hochgradiger Mikrophthalmus beim Patau-Syndrom. Klin Monatsbl Augenheilkd 1978;173:342-7.","journal-title":"Klin Monatsbl Augenheilkd"},{"key":"ref_5","first-page":"406","article-title":"A case report with no extracranial abnormalities and normal chromosome count and karyotype","volume":"65","author":"Bishop, K.; Connolly, J.M.; Carter, C.H.; Holoprosencephaly, Carpenter D.G.","year":"1964","unstructured":"Bishop K, Connolly JM, Carter CH, Carpenter DG. Holoprosencephaly. A case report with no extracranial abnormalities and normal chromosome count and karyotype. J Pediatr 1964;65:406-14.","journal-title":"J Pediatr"},{"key":"ref_6","first-page":"556","article-title":"Features of 13-15 trisomy syndrome with normal karyotype","volume":"1","year":"1964","unstructured":"Marshall R, Newnham RE, Rawstron JR, Ellis JR, Stevens LJ. Features of 13-15 trisomy syndrome with normal karyotype. Lancet 1964;1:556.","journal-title":"Lancet"},{"key":"ref_7","first-page":"3","article-title":"A hereditary sublethal syndrome in man. Skr Norske Vidensk Akad Mat Nat Kl","volume":"14","author":"Mohr, O.L.","year":"1941","unstructured":"Mohr OL. A hereditary sublethal syndrome in man. Skr Norske Vidensk Akad Mat Nat Kl 1941;14:3-17."},{"key":"ref_8","first-page":"1147","article-title":"Et arvelig syndrom omfattende tungemisdannelse og polydactyli","volume":"30","author":"0, Claussen","year":"1946","unstructured":"Claussen 0. Et arvelig syndrom omfattende tungemisdannelse og polydactyli. Nord Med 1946;30:1147-51.","journal-title":"Nord Med"},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1016\/S0022-3476(67)80236-1","article-title":"Genetic and clinical heterogeneity in the oral-facial-digital syndromes","volume":"71","author":"Rimoin, D.L.; Edgerton, M.T.","year":"1967","unstructured":"Rimoin DL, Edgerton MT. Genetic and clinical heterogeneity in the oral-facial-digital syndromes. J Pediatr 1967;71:94-102.","journal-title":"J Pediatr"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1111\/j.1399-0004.1971.tb00287.x","article-title":"Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome)","volume":"2","author":"Gustavson, K.H.; Kreuger, A.; Petersson, P.O.","year":"1971","unstructured":"Gustavson KH, Kreuger A, Petersson PO. Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome). 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