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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

225 related items for PubMed ID: 8291524

  • 41.
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  • 43. Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
    al-Gazali LI, al-Talabani J.
    Clin Dysmorphol; 1996 Jul; 5(3):249-53. PubMed ID: 8818454
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  • 49. The Brachmann-de Lange syndrome.
    Opitz JM.
    Am J Med Genet; 1985 Sep; 22(1):89-102. PubMed ID: 3901753
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  • 52. Partial trisomy 4p and Brachmann-de Lange syndrome.
    Fryns JP.
    Am J Med Genet; 2000 Dec 11; 95(4):406. PubMed ID: 11186901
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  • 53. Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome.
    Breslau EJ, Disteche C, Hall JG, Thuline H, Cooper P.
    Am J Med Genet; 1981 Dec 11; 10(2):179-86. PubMed ID: 7315874
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  • 56. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance.
    Hordijk R, Van de Logt F, Houtman WA, Van Essen AJ.
    Genet Couns; 1996 Dec 11; 7(2):113-22. PubMed ID: 8831130
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