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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

226 related items for PubMed ID: 6930994

  • 1.
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  • 2. Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis.
    Cohen MM, Jirásek JE, Guzman RT, Gorlin RJ, Peterson MQ.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):125-35. PubMed ID: 5173200
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  • 3. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
    Corsello G, Buttitta P, Cammarata M, Lo Presti A, Maresi E, Zumpani L, Giuffrè L.
    Am J Med Genet; 1990 Oct; 37(2):244-9. PubMed ID: 2147361
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  • 4. Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.
    van Essen AJ, Schoots CJ, van Lingen RA, Mourits MJ, Tuerlings JH, Leegte B.
    Am J Med Genet; 1993 Aug 01; 47(1):85-8. PubMed ID: 8368259
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  • 5. Median facial malformations and their implications for brain malformations.
    DeMyer W.
    Birth Defects Orig Artic Ser; 1975 Aug 01; 11(7):155-81. PubMed ID: 764897
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  • 6. Holoprosencephaly and septo-optic dysplasia.
    Fitz CR.
    Neuroimaging Clin N Am; 1994 May 01; 4(2):263-81. PubMed ID: 8081628
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  • 7. Alobar holoprosencephaly associated with cebocephaly and craniosynostosis.
    Lin CH, Tsai JD, Ho YJ, Lin WC.
    Acta Neurol Taiwan; 2009 Jun 01; 18(2):123-6. PubMed ID: 19673365
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  • 10. [Aarskog's genito-digito-facial syndrome].
    Fouanon C, André MJ, Gillot F.
    Bull Soc Ophtalmol Fr; 1976 Nov 01; 76(11):981-5. PubMed ID: 1030364
    [No Abstract] [Full Text] [Related]

  • 11. Two new familial cases of the G syndrome.
    Frias JL, Rosenbloom AL.
    Birth Defects Orig Artic Ser; 1975 Nov 01; 11(2):54-7. PubMed ID: 1227574
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  • 12. Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].
    Schwartz S, Meekins J, Panny SR, Sun CC, Cohen MM.
    Am J Med Genet; 1983 May 01; 15(1):141-4. PubMed ID: 6859113
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  • 14. An unusual case of median cleft lip with orbital hypotelorism--a missing link in the classification.
    Ben-Hur N, Ashur H, Murreri M.
    Cleft Palate J; 1978 Oct 01; 15(4):365-8. PubMed ID: 281280
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  • 15. Microscopic study of holoprosencephalic facial anomalies in trisomy 13 fetuses.
    Sperber GH, Honoré LH, Machin GA.
    Am J Med Genet; 1989 Apr 01; 32(4):443-51. PubMed ID: 2773983
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  • 16. [Holoprosencephaly--clinical picture and genetic counseling in 6 cases].
    Brackertz M, Schindler D, Grimm T, Zahn V.
    Klin Padiatr; 1985 Apr 01; 197(1):50-7. PubMed ID: 2983145
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  • 18. [Associated morphological anomalies of the face and brain in infants].
    Couly G, Aicardi J.
    Arch Fr Pediatr; 1988 Feb 01; 45(2):99-104. PubMed ID: 3389979
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