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Journal Abstract Search

360 related items for PubMed ID: 9852671

  • 1. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M, Sugio Y.
    J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
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  • 4. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F.
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
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  • 6. Autosomal dominant microcephaly with mental retardation.
    Bawle E, Horton M.
    Am J Med Genet; 1989 Jul; 33(3):382-4. PubMed ID: 2801773
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  • 7. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML, Martín M, Pardo M, Fernandez de las Heras F, Frías JL.
    Am J Med Genet; 1995 Jan 16; 55(2):213-6. PubMed ID: 7717420
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  • 8. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M, Ito M, Hall BD.
    Am J Med Genet; 1984 Jan 16; 17(1):367-74. PubMed ID: 6711604
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  • 9. The syndrome of Hirschsprung disease, microcephaly, unusual face, and mental retardation.
    Halal F, Morel J.
    Am J Med Genet; 1990 Sep 16; 37(1):106-8. PubMed ID: 2240026
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  • 11. Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome.
    Verloes A, Lesenfants S, Philippet B, Iyawa A, Laloux F, Koulischer L.
    Genet Couns; 1996 Sep 16; 7(4):277-82. PubMed ID: 8985731
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  • 12. Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.
    Chudley AE, Lowry RB, Hoar DI.
    Am J Med Genet; 1988 Dec 16; 31(4):741-51. PubMed ID: 3239563
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  • 13. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
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  • 14. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C.
    Am J Med Genet; 1990 Sep 15; 37(1):119-23. PubMed ID: 2240028
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  • 15. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
    Seemanová E, Lesný I.
    Am J Med Genet; 1996 Dec 11; 66(2):179-83. PubMed ID: 8958326
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  • 16. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.
    Weaver DD, Williams CP.
    Birth Defects Orig Artic Ser; 1977 Dec 11; 13(3B):69-84. PubMed ID: 890101
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  • 17. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y, Kajii T.
    Am J Med Genet; 1984 Dec 11; 19(4):741-53. PubMed ID: 6517098
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  • 18. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A, Schinzel A.
    Clin Dysmorphol; 1993 Jul 11; 2(3):225-31. PubMed ID: 8287184
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  • 19. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
    Bibas Bonet H, Fontenla M, Fauze R, G de Pinat I.
    Rev Neurol; 1993 Jul 11; 32(8):746-50. PubMed ID: 11391511
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  • 20. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family.
    Wulfsberg EA, Campbell AB, Lurie IW, Eanet KR.
    Am J Med Genet; 1996 Jun 28; 63(4):554-7. PubMed ID: 8826434
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