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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
327 related items for PubMed ID: 8031535
1. Syndactyly of the ring and small finger. De Smet L, Mulier T, Fabry G. Genet Couns; 1994; 5(1):45-9. PubMed ID: 8031535 [Abstract] [Full Text] [Related]
2. An autosomal dominant syndrome of renal and anogenital malformations with syndactyly. Green AJ, Sandford RN, Davison BC. J Med Genet; 1996 Jul; 33(7):594-6. PubMed ID: 8818947 [Abstract] [Full Text] [Related]
3. Variable expression of isolated familial long-ring-little syndactyly. Al-Qattan MM. J Hand Surg Br; 2000 Aug; 25(4):400-2. PubMed ID: 11058014 [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 Aug; 6(1):51-9. PubMed ID: 4372010 [No Abstract] [Full Text] [Related]
5. Type II syndactyly or synpolydactyly. De Smet L, Fabry G. Acta Orthop Belg; 1992 Aug; 58(2):209-12. PubMed ID: 1321548 [Abstract] [Full Text] [Related]
11. [Syndactylia associated with multiple malformation syndromes. Observation of a new symptomatologic complex in 3 brothers]. Garau A, Nurchi AM, Melis P, Frau G, Costa G. Pediatr Med Chir; 1988 Jan; 10(2):227-32. PubMed ID: 2845373 [Abstract] [Full Text] [Related]
12. Chromosome abnormalities in patients with syndactyly. Conen PE, Hampole MK, Thomson HG. Can Med Assoc J; 1969 Nov 15; 101(10):75-8. PubMed ID: 4310631 [Abstract] [Full Text] [Related]
13. [Molecular advances in "non-mendelian" genetics. Implications for pediatrics]. Pérez Jurado LA. An Esp Pediatr; 1993 Jun 15; 38(6):479-87. PubMed ID: 8368674 [No Abstract] [Full Text] [Related]
14. The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a family. Ioan DM, Dumitriu L, Belengeariu V, Fryns JP. Genet Couns; 1997 Jun 15; 8(2):87-90. PubMed ID: 9219005 [Abstract] [Full Text] [Related]
15. Hallux syndactyly--ulnar polydactyly--abnormal ear lobes: a new syndrome. Goldberg MJ, Pashayan HM. Birth Defects Orig Artic Ser; 1976 Jun 15; 12(5):255-66. PubMed ID: 182299 [Abstract] [Full Text] [Related]
16. [A new autosomal-recessive hereditary syndrome. Multiple peripheral pulmonary stenosis, brachytelephalangia, inner-ear deafness, ossification or calcification of cartilages]. Keutel J, Jörgensen G, Gabriel P. Dtsch Med Wochenschr; 1971 Oct 22; 96(43):1676-81 passim. PubMed ID: 5099199 [No Abstract] [Full Text] [Related]
17. Congenital defects of the breast - an autosomal dominant trait. Nelson MM, Cooper CK. S Afr Med J; 1982 Mar 20; 61(12):434-6. PubMed ID: 7064019 [Abstract] [Full Text] [Related]
18. [Current indications for chromosome study in congenital defects]. de la Chapelle A, Kääriäinen H, Salonen R. Duodecim; 1981 Mar 20; 97(16):1320-32. PubMed ID: 7327123 [No Abstract] [Full Text] [Related]
19. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes. Robin NH, Segel B, Carpenter G, Muenke M. Am J Med Genet; 1996 Mar 15; 62(2):184-91. PubMed ID: 8882401 [Abstract] [Full Text] [Related]
20. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly]. Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L. Yi Chuan Xue Bao; 2003 Oct 15; 30(10):973-7. PubMed ID: 14669516 [Abstract] [Full Text] [Related] Page: [Next] [New Search]