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PUBMED FOR HANDHELDS

Journal Abstract Search

165 related items for PubMed ID: 4462626

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  • 3. Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
    Frank Y, Ziprkowski M, Romano A, Stein R, Katznelson MB, Cohen B, Goodman RM.
    J Genet Hum; 1973 Jun; 21(2):67-72. PubMed ID: 4805907
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  • 4. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
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  • 5. Gastro-cutaneous syndrome: peptic ulcer/hiatal hernia, multiple lentigines/café-au-lait spots, hypertelorism, and myopia.
    Halal F, Gervais MH, Baillargeon J, Lesage R.
    Am J Med Genet; 1982 Feb; 11(2):161-76. PubMed ID: 7065007
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  • 13. Two new familial cases of the G syndrome.
    Frias JL, Rosenbloom AL.
    Birth Defects Orig Artic Ser; 1975 Feb; 11(2):54-7. PubMed ID: 1227574
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  • 16. [Familial and hereditary microcephaly. Study of 10 cases in 4 families].
    Bost M, Crouzet G, Jalbert P, Lesage A, Beaudoing A.
    Pediatrie; 1971 Sep; 26(6):587-98. PubMed ID: 5116340
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  • 17. [The Greig syndrome].
    Fehlow P.
    Kinderarztl Prax; 1984 Mar; 52(3):145-9. PubMed ID: 6727153
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  • 20. [Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion].
    Naffah J, Ghosn G, Gharios N.
    Arch Fr Pediatr; 1972 Dec; 29(10):1069-81. PubMed ID: 4662280
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