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Journal Abstract Search

354 related items for PubMed ID: 19554981

  • 21. The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
    Mendez HM, Paskulin GA, Vallandro C.
    Am J Med Genet; 1985 Oct; 22(2):223-8. PubMed ID: 4050854
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  • 22. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L, El-Nabi MM, Azab AS, Gouda SA, Al-Wadaani AM, Naguib KK.
    East Mediterr Health J; 2007 Oct; 13(4):975-9. PubMed ID: 17955782
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  • 25. Brief clinical report: an X-linked mental retardation syndrome with craniofacial abnormalities, microcephaly and club foot.
    Holmes LB, Gang DL.
    Am J Med Genet; 1984 Jan; 17(1):375-82. PubMed ID: 6711605
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  • 29. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
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  • 30. Dubowitz syndrome: a cholesterol metabolism disorder?
    Yeşilkaya E, Karaer K, Bideci A, Camurdan O, Perçin EF, Cinaz P.
    Genet Couns; 2008 Feb 01; 19(3):287-90. PubMed ID: 18990984
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  • 32. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 01; 141(7):584-6. PubMed ID: 8413337
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