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Journal Abstract Search

254 related items for PubMed ID: 9679615

  • 41. Delineation of the da-Silva syndrome.
    Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K.
    Am J Med Genet; 1994 Feb 01; 49(3):313-6. PubMed ID: 8209892
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  • 42. [Smith-Lemli-Opitz Syndrome; endocrinologic study (author's transl)].
    Muñoz Calvo MT, Ceñal González MJ, Parra Martínez I, Hervás Olivares F, Nieto Cuartero JA, Lestache RG.
    An Esp Pediatr; 1981 Nov 01; 15(5):498-502. PubMed ID: 7332154
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  • 44. Opitz trigonocephaly syndrome.
    Haaf T, Hofmann R, Schmid M.
    Am J Med Genet; 1991 Sep 15; 40(4):444-6. PubMed ID: 1746609
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  • 46. Clinical and behavioral characteristics in FG syndrome.
    Graham JM, Superneau D, Rogers RC, Corning K, Schwartz CE, Dykens EM.
    Am J Med Genet; 1999 Aug 27; 85(5):470-5. PubMed ID: 10405444
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  • 47. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
    Lungarotti MS, Martello C, Barboni G, Mezzetti D, Mariotti G, Calabro A.
    Am J Med Genet; 1994 Jul 15; 51(4):598-601. PubMed ID: 7943046
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  • 49. Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?
    Kirel B, Kural N, Yakut A, Adapinar B.
    Turk J Pediatr; 2000 Jul 15; 42(2):171-6. PubMed ID: 10936989
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  • 50. Dubowitz syndrome: a defect in the cholesterol biosynthetic pathway?
    Ahmad A, Amalfitano A, Chen YT, Kishnani PS, Miller C, Kelley R.
    Am J Med Genet; 1999 Oct 29; 86(5):503-4. PubMed ID: 10508998
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  • 59. Smith-Lemli-Opitz syndrome: a treatable inherited error of metabolism causing mental retardation.
    Nowaczyk MJ, Whelan DT, Heshka TW, Hill RE.
    CMAJ; 1999 Jul 27; 161(2):165-70. PubMed ID: 10439827
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  • 60. Smith-Lemli-Opitz syndrome.
    Sinclair L, Winterborn MH, Brown J.
    Proc R Soc Med; 1969 Sep 27; 62(9):907-8. PubMed ID: 5349196
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