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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
127 related items for PubMed ID: 3981586
1. Familial opposable triphalangeal thumbs associated with duplication of the big toes. Merlob P, Grunebaum M, Reisner SH. J Med Genet; 1985 Feb; 22(1):78-80. PubMed ID: 3981586 [Abstract] [Full Text] [Related]
2. Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance. Silengo MC, Biagioli M, Bell GL, Bona G, Franceschini P. Clin Genet; 1987 Jan; 31(1):13-8. PubMed ID: 3568429 [Abstract] [Full Text] [Related]
3. Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis. Canún S, Lomelí RM, Martínez R, Carnevale A. Clin Genet; 1984 Feb; 25(2):182-6. PubMed ID: 6705252 [Abstract] [Full Text] [Related]
4. A syndrome of polydactyly-syndactyly and triphalangeal thumbs in three generations. Yujnovsky O, Ayala D, Vincitorio A, Viale H, Sakati N, Nyhan WL. Clin Genet; 1974 Feb; 6(1):51-9. PubMed ID: 4372010 [No Abstract] [Full Text] [Related]
5. A new syndrome of triphalangeal thumbs and brachy-ectrodactyly. Carnevale A, Hernández M, del Castillo V, Torres P. Clin Genet; 1980 Oct; 18(4):244-52. PubMed ID: 7438506 [Abstract] [Full Text] [Related]
6. Distal symphalangism with involvement of the thumbs and great toes. Matthews S, Farnish S, Young ID. Clin Genet; 1987 Dec; 32(6):375-8. PubMed ID: 3436086 [Abstract] [Full Text] [Related]
7. Autosomal dominant transmission of bilateral "opposable" triphalangeal thumb. Merolli A, Tranquilli Leali P, Cataldi L. Chir Organi Mov; 1999 Dec; 84(4):381-6. PubMed ID: 11569006 [Abstract] [Full Text] [Related]
8. Opposable triphalangeal thumb: clinical features and results of treatment. Ogino T, Ishii S, Kato H. J Hand Surg Am; 1994 Jan; 19(1):39-47. PubMed ID: 8169367 [Abstract] [Full Text] [Related]
9. Stub thumbs in Israel revisited. Goodman RM, Feinstein A, Hertz M. J Med Genet; 1984 Dec; 21(6):460-2. PubMed ID: 6512836 [Abstract] [Full Text] [Related]
10. Non-opposable triphalangeal thumb in an Italian family. Warm A, Di Pietro C, D'Agrosa F, Cambiè M, Gaboardi F. J Med Genet; 1988 May; 25(5):337-9. PubMed ID: 3385742 [Abstract] [Full Text] [Related]
11. Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly. Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB. Am J Med Genet A; 2007 Jan 01; 143A(1):27-32. PubMed ID: 17152067 [Abstract] [Full Text] [Related]
12. [Triphalangeal thumb. Apropos of a case]. Núñez Motilva ME, González ML, Sarriá Chueca A, Villavieja Atance JL, Jiménez A. An Esp Pediatr; 1985 Mar 31; 22(4):335-7. PubMed ID: 4003961 [No Abstract] [Full Text] [Related]
13. Pfeiffer syndrome. An unusual type of acrocephalosyndactyly with broad thumbs and great toes. Martsolf JT, Cracco JB, Carpenter GG, O'Hara AE. Am J Dis Child; 1971 Mar 31; 121(3):257-62. PubMed ID: 5551881 [No Abstract] [Full Text] [Related]
14. A novel frameshift mutation of the GLI3 gene in a family with broad thumbs with/without big toes, postaxial polydactyly and variable syndactyly of the hands/feet. Al-Qattan MM. Clin Genet; 2012 Nov 31; 82(5):502-4. PubMed ID: 22428873 [No Abstract] [Full Text] [Related]
15. Triphalangeal thumb. Miura T. Plast Reconstr Surg; 1976 Nov 31; 58(5):587-94. PubMed ID: 981404 [Abstract] [Full Text] [Related]
16. Aplasia of the thumbs and great toes as the outstanding feature of Yunis and Varon syndrome. A new entity. A new observation. Pfeiffer RA, Diekmann L, Stock HJ. Ann Genet; 1988 Nov 31; 31(4):241-3. PubMed ID: 3265308 [Abstract] [Full Text] [Related]
17. Dominant inheritance of a syndrome similar to Rubinstein-Taybi. Cotsirilos P, Taylor JC, Matalon R. Am J Med Genet; 1987 Jan 31; 26(1):85-93. PubMed ID: 3812583 [Abstract] [Full Text] [Related]
18. Polydactyly: a study of a five generation Indian family. Radhakrishna U, Multani AS, Solanki JV, Shah VC, Chinoy NJ. J Med Genet; 1993 Apr 31; 30(4):296-9. PubMed ID: 8487274 [Abstract] [Full Text] [Related]
19. [Three-phalangeal thumbs]. Salon A. Chir Main; 2008 Dec 31; 27 Suppl 1():S71-81. PubMed ID: 18930429 [Abstract] [Full Text] [Related]
20. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin. Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM. Am J Hum Genet; 2002 Sep 31; 71(3):618-24. PubMed ID: 12089654 [Abstract] [Full Text] [Related] Page: [Next] [New Search]