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22. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome? Belengeanu V, Rozsnyai K, Farcaş S, Velea I, Fryns JP. Genet Couns; 2005 Jun; 16(2):167-71. PubMed ID: 16080297 [Abstract] [Full Text] [Related]
23. Short rib-polydactyly syndrome, Majewski type. Chen H, Yang SS, Gonzalez E, Fowler M, Al Saadi A. Am J Med Genet; 1980 Jun; 7(2):215-22. PubMed ID: 7468649 [Abstract] [Full Text] [Related]
24. Autosomal recessive omodysplasia. Stoll C, Pennerath A, Poirat P. Ann Genet; 1995 Jun; 38(2):97-101. PubMed ID: 7486832 [Abstract] [Full Text] [Related]
27. Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia. Chemke J, Carmi R, Galil A, Bar-Ziv Y, Ben-Ytzhak I, Zurkowski L. Am J Med Genet; 1992 Aug 01; 43(6):989-95. PubMed ID: 1415350 [Abstract] [Full Text] [Related]
30. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family. Gollop TR, Colletto GM. Am J Med Genet; 1984 Feb 01; 17(2):399-406. PubMed ID: 6702893 [Abstract] [Full Text] [Related]
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35. Autosomal recessive form of whistling face syndrome in sibs. Dallapiccola B, Giannotti A, Lembo A, Saguì L. Am J Med Genet; 1989 Aug 01; 33(4):542-4. PubMed ID: 2596515 [Abstract] [Full Text] [Related]