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Journal Abstract Search

172 related items for PubMed ID: 7681735

  • 1. Guadalajara camptodactyly syndrome type I. A corroborative family.
    Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM.
    Clin Genet; 1993 Jan; 43(1):11-5. PubMed ID: 7681735
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  • 3. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
    Pena SD, Shokeir MH.
    Birth Defects Orig Artic Ser; 1976 Jan; 12(5):201-8. PubMed ID: 953225
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  • 5. Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.
    Goodman RM, Katznelson MB, Hertz M, Katznelson A.
    J Med Genet; 1976 Apr; 13(2):136-41. PubMed ID: 933111
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  • 8. Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: autosomal recessive entity?
    Kilic I, Kilic BA, Ergin H, Aygün MG, Aksit MA.
    Am J Med Genet; 1998 Apr 28; 77(1):28-30. PubMed ID: 9557890
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  • 14. Greig cephalopolysyndactyly: report of 13 affected individuals in three families.
    Baraitser M, Winter RM, Brett EM.
    Clin Genet; 1983 Oct 28; 24(4):257-65. PubMed ID: 6641002
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  • 15. Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes: a possible new autosomal recessive disorder.
    Gül D, Oktenli C, Sağlam M, Erdem U.
    Clin Dysmorphol; 2000 Jan 28; 9(1):61-2. PubMed ID: 10649801
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  • 18. Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome.
    Roifman CM, Chitayat D.
    Clin Genet; 2009 Nov 28; 76(5):449-57. PubMed ID: 19863561
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  • 20. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.
    Clayton-Smith J, Donnai D.
    J Med Genet; 1989 May 28; 26(5):339-42. PubMed ID: 2732996
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