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Journal Abstract Search

341 related items for PubMed ID: 6711604

  • 1. 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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  • 2. A new X-linked mental retardation-overgrowth syndrome.
    Golabi M, Rosen L.
    Am J Med Genet; 1984 Jan; 17(1):345-58. PubMed ID: 6538755
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  • 3. 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; 36(1):89-93. PubMed ID: 2333912
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  • 4. 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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  • 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. 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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  • 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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  • 12. 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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  • 13. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS, Wisniewski K, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):586-90. PubMed ID: 7943044
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  • 14. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F.
    Am J Med Genet; 1983 May 15; 15(1):135-40. PubMed ID: 6859112
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  • 17. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
    Riccardi VM, Hässler E, Lubinsky MS.
    Am J Med Genet; 1977 May 15; 1(1):47-58. PubMed ID: 565138
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  • 18. A form of X-linked mental retardation with marfanoid habitus.
    Lujan JE, Carlin ME, Lubs HA.
    Am J Med Genet; 1984 Jan 15; 17(1):311-22. PubMed ID: 6711603
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  • 19. The syndrome of Hirschsprung disease, microcephaly, unusual face, and mental retardation.
    Halal F, Morel J.
    Am J Med Genet; 1990 Sep 15; 37(1):106-8. PubMed ID: 2240026
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