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Pubmed for Handhelds

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Journal Abstract Search

208 related items for PubMed ID: 6999382

  • 21.
    ; . PubMed ID:
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  • 22. Neuroblastoma in patients with constitutional chromosomal changes.
    Fryns JP.
    Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
    [No Abstract] [Full Text] [Related]

  • 23. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
    Sarda P, Lefort G, Devaux P, Humeau C, Rieu D.
    Ann Genet; 1992; 35(2):117-20. PubMed ID: 1524409
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  • 28. [Wolf syndrome. Apropos of 2 cases].
    García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V.
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
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  • 30. An unusual ocular finding associated with chromosome 1q deletion syndrome.
    Wright LL, Schwartz MF, Schwartz S, Karesh J.
    Pediatrics; 1986 May; 77(5):786. PubMed ID: 3703649
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  • 31.
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  • 32. Familial chromosomal aberrations. I.
    Zellweger H.
    Ann Paediatr; 1966 May; 206(5):317-32. PubMed ID: 4225154
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  • 33. Chromosomal abnormalities in clinical medicine.
    Carr DH.
    Prog Med Genet; 1969 May; 6():1-61. PubMed ID: 4241258
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  • 39. [The practicing physician facing current problems in genetics].
    Juillard E, Grosset L.
    Rev Med Suisse Romande; 1973 Sep; 93(9):655-68. PubMed ID: 4272167
    [No Abstract] [Full Text] [Related]

  • 40. Genetic counselling for neurological disorders.
    Sutherland GR.
    Aust Fam Physician; 1979 Dec; 8(12):1265-72. PubMed ID: 161168
    [Abstract] [Full Text] [Related]

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