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Journal Abstract Search

440 related items for PubMed ID: 8723107

  • 1. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
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  • 2. Syndactyly type IV/hexadactyly of feet associated with unilateral absence of the tibia.
    Rambaud-Cousson A, Dudin AA, Zuaiter AS, Thalji A.
    Am J Med Genet; 1991 Aug 01; 40(2):144-5. PubMed ID: 1654744
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  • 4. Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian family.
    Richieri-Costa A, Brunoni D, Laredo Filho J, Kasinski S.
    Am J Med Genet; 1987 Dec 01; 28(4):971-80. PubMed ID: 3688036
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  • 5. Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred.
    Ahmad M, Abbas H, Wahab A, Haque S.
    Am J Med Genet; 1990 Jul 01; 36(3):292-6. PubMed ID: 2363425
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  • 10. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Jul 01; 13(2):210-3. PubMed ID: 8459013
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  • 11. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.
    Sayli BS, Akarsu AN, Sayli U, Akhan O, Ceylaner S, Sarfarazi M.
    J Med Genet; 1995 Jun 01; 32(6):421-34. PubMed ID: 7666393
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  • 12. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
    Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W.
    Clin Genet; 2012 Jul 01; 82(1):48-55. PubMed ID: 21554266
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  • 14. Familial occurrence of bifid femur and monodactylous ectrodactyly.
    Gollop TR, Lucchesi E, Martins RM, Nione AS.
    Am J Med Genet; 1980 Jul 01; 7(3):319-22. PubMed ID: 7468656
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  • 15. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
    Am J Med Genet; 1991 Nov 01; 41(2):141-52. PubMed ID: 1785624
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  • 17. A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
    Akarsu AN, Akhan O, Sayli BS, Sayli U, Baskaya G, Sarfarazi M.
    J Med Genet; 1995 Jun 01; 32(6):435-41. PubMed ID: 7666394
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  • 19. [Hypoplasia of the tibia, polydactyly, and triphalangeal thumb: 1st family described in Venezuela].
    Martínez-Basalo C, González-Inciarte ME, Delgado-Luengo W, Casilla-Nava S, González-Incíarte L, Alvarez-Nava F, Boscán-Porras N, Delgado-Luengo J.
    Invest Clin; 1997 Dec 01; 38(4):219-26. PubMed ID: 9527389
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