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Journal Abstract Search

327 related items for PubMed ID: 6711605

  • 1. 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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  • 2. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M, Ito M, Hall BD.
    Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604
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  • 3. 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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  • 4. 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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  • 5. 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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  • 6. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M, Sugio Y.
    J Hum Genet; 1998 Sep 15; 43(4):224-7. PubMed ID: 9852671
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  • 9. A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
    Schimke RN, Horton WA, Collins DL, Therou L.
    Am J Med Genet; 1984 Jan 15; 17(1):323-32. PubMed ID: 6538752
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  • 10. 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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  • 13. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May 01; 36(1):89-93. PubMed ID: 2333912
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  • 18. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
    Martínez-Garay I, Tomás M, Oltra S, Ramser J, Moltó MD, Prieto F, Meindl A, Kutsche K, Martínez F.
    Eur J Hum Genet; 2007 Jan 01; 15(1):29-34. PubMed ID: 17033686
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