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Journal Abstract Search

207 related items for PubMed ID: 7473658

  • 1. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC, Thomas PS, Eedy DJ, Shepherd C.
    J Med Genet; 1995 Aug; 32(8):638-41. PubMed ID: 7473658
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  • 2. Cooks syndrome: a case report and brief review.
    Brennan CB, Buehler T, Lesher JL.
    Pediatr Dermatol; 2013 Aug; 30(4):e52-3. PubMed ID: 22329539
    [Abstract] [Full Text] [Related]

  • 3. A new nail dysplasia syndrome with onychonychia and absence and/or hypoplasia of distal phalanges.
    Cooks RG, Hertz M, Katznelson MB, Goodman RM.
    Clin Genet; 1985 Jan; 27(1):85-91. PubMed ID: 3978841
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  • 4. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
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  • 8. Clinical and molecular studies of brachydactyly type D.
    Robin NH, Hurvitz J, Warman ML, Morrison S.
    Am J Med Genet; 1999 Aug 06; 85(4):413-8. PubMed ID: 10398270
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  • 9. Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.
    Ausems MG, Ippel PF, Renardel de Lavalette PA.
    Clin Dysmorphol; 1994 Jan 06; 3(1):21-30. PubMed ID: 8205322
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  • 10. Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred.
    Wallis CE.
    Clin Genet; 1988 Oct 06; 34(4):252-7. PubMed ID: 3233778
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  • 12. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M, Schapera J.
    Eur J Pediatr; 1988 Feb 06; 147(2):202-5. PubMed ID: 3366140
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  • 13. F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family.
    Camera G, Camera A, Pozzolo S, Costa M, Mantero R.
    Am J Med Genet; 1995 Jul 03; 57(3):472-5. PubMed ID: 7677153
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  • 15. Familial combination of brachydactyly, type E and atrial septal defect, type II.
    Czeizel A, Göblyös P.
    Eur J Pediatr; 1989 Nov 03; 149(2):117-9. PubMed ID: 2591402
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  • 16. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD, Dowton SB, McAlister WH, Waggoner DJ.
    Clin Genet; 2000 Jun 03; 57(6):444-8. PubMed ID: 10905665
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  • 17. Acrodysostosis in two generations: an autosomal dominant syndrome.
    Hernández RM, Miranda A, Kofman-Alfaro S.
    Clin Genet; 1991 May 03; 39(5):376-82. PubMed ID: 1860254
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  • 18. Clinical and locus heterogeneity in brachydactyly type C.
    Robin NH, Gunay-Aygun M, Polinkovsky A, Warman ML, Morrison S.
    Am J Med Genet; 1997 Jan 31; 68(3):369-77. PubMed ID: 9024575
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