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Journal Abstract Search

450 related items for PubMed ID: 6859112

  • 1. 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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  • 2. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.
    Weaver DD, Williams CP.
    Birth Defects Orig Artic Ser; 1977 May; 13(3B):69-84. PubMed ID: 890101
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  • 5. 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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  • 7. Familial holoprosencephaly.
    Dallaire L, Fraser FC, Wiglesworth FW.
    Birth Defects Orig Artic Ser; 1971 Jun 15; 7(7):136-42. PubMed ID: 5173201
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  • 8. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM, Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1993 Sep 01; 47(3):330-2. PubMed ID: 8135276
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  • 9. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 01; 16(4):475-80. PubMed ID: 6660246
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  • 10. The Gordon syndrome: autosomal dominant cleft palate, camptodactyly, and club feet.
    Robinow M, Johnson GF.
    Am J Med Genet; 1981 Dec 01; 9(2):139-46. PubMed ID: 7258227
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  • 11. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A, Colletto GM, Gollop TR, Masiero D.
    Am J Med Genet; 1985 Apr 01; 20(4):631-8. PubMed ID: 2986457
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  • 12. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M, Sugio Y.
    J Hum Genet; 1998 Apr 01; 43(4):224-7. PubMed ID: 9852671
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  • 16. 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 01; 17(1):375-82. PubMed ID: 6711605
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  • 17. Short stature, mental retardation, eye anomalies, and cleft lip/palate.
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1992 Feb 15; 42(4):449-52. PubMed ID: 1609826
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  • 18. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L, Sorge G, Pavone V, Rizzo R, Ruggieri M, Polizzi A, Opitz JM.
    Am J Med Genet; 1997 Aug 22; 71(3):271-4. PubMed ID: 9268094
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  • 19. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M, Ito M, Hall BD.
    Am J Med Genet; 1984 Jan 22; 17(1):367-74. PubMed ID: 6711604
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  • 20. Ocular hypotelorism, submucosal cleft palate, and hypospadias: a new autosomal dominant syndrome.
    Schilbach U, Rott HD.
    Am J Med Genet; 1988 Dec 22; 31(4):863-70. PubMed ID: 3149147
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