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29. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II. Blanchet P; Lefort G; Eglin MC; Rieu D; Sarda P Genet Couns; 1993; 4(4):289-94. PubMed ID: 8110417 [TBL] [Abstract][Full Text] [Related]
30. Silver-Russell syndrome with absence of digits and syndactylism of the fingers. Keppen LD; Rennert OM Clin Genet; 1983 Dec; 24(6):453-5. PubMed ID: 6317237 [TBL] [Abstract][Full Text] [Related]
31. Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes. Malik S; Afzal M; Gul S; Wahab A; Ahmad M Am J Med Genet A; 2010 Sep; 152A(9):2313-7. PubMed ID: 20683984 [TBL] [Abstract][Full Text] [Related]
32. Poly-syndactyly of hands and feet with talipes equino-varus. An unusual combination. Gadegone WM; Kumar K J Hand Surg Br; 1984 Jun; 9(2):149-50. PubMed ID: 6086792 [TBL] [Abstract][Full Text] [Related]
33. Anomalies of the fingers and toes associated with Klippel-Trenaunay syndrome. McGrory BJ; Amadio PC; Dobyns JH; Stickler GB; Unni KK J Bone Joint Surg Am; 1991 Dec; 73(10):1537-46. PubMed ID: 1660897 [TBL] [Abstract][Full Text] [Related]
34. Opitz trigonocephaly syndrome and terminal transverse limb reduction defects. Fryns JP; Snoeck L; Kleczkowska A; Van den Berghe H Helv Paediatr Acta; 1985; 40(6):485-8. PubMed ID: 3830973 [TBL] [Abstract][Full Text] [Related]
35. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)]. Scheffer P; Verdier M; Finidori G Rev Stomatol Chir Maxillofac; 1981; 82(4):230-3. PubMed ID: 6944759 [TBL] [Abstract][Full Text] [Related]
36. O--short stature with abnormalities of the cranium and limbs. Jorgenson RJ Birth Defects Orig Artic Ser; 1974; 10(5):249-51. PubMed ID: 4469995 [No Abstract] [Full Text] [Related]
38. Three siblings with similar anomalies in the eyes, bones and skin. Tuomaala P; Haapanen E Acta Ophthalmol (Copenh); 1968; 46(3):365-71. PubMed ID: 4974459 [No Abstract] [Full Text] [Related]
39. The craniodigital syndrome of Scott: report of a second family. Lorenz P; Hinkel GK; Hoffmann C; Rupprecht E Am J Med Genet; 1990 Oct; 37(2):224-6. PubMed ID: 2174209 [TBL] [Abstract][Full Text] [Related]
40. Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity. Genuardi M; Zollino M; Bellussi A; Fuhrmann W; Neri G Clin Genet; 1990 Nov; 38(5):321-6. PubMed ID: 2178076 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]