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Journal Abstract Search

180 related items for PubMed ID: 3121220

  • 1. X-linked dysmorphic syndrome with mental retardation.
    Prieto F, Badía L, Mulas F, Monfort A, Mora F.
    Clin Genet; 1987 Nov; 32(5):326-34. PubMed ID: 3121220
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  • 2. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
    Hyde-Forster I, McCarthy G, Berry AC.
    J Med Genet; 1992 Oct; 29(10):736-8. PubMed ID: 1433236
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  • 3. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
    Watty A, Prieto F, Beneyto M, Neugebauer M, Gal A.
    Am J Med Genet; 1991 Oct; 38(2-3):234-9. PubMed ID: 1673297
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  • 4. Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.
    Guerrini R, Dobyns WB.
    Neurology; 1998 Aug; 51(2):499-503. PubMed ID: 9710025
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  • 6. X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq.
    Carpenter NJ, Qu Y, Curtis M, Patil SR.
    Am J Med Genet; 1999 Jul 30; 85(3):230-5. PubMed ID: 10398234
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  • 10. Corpus callosum agenesis, spastic quadriparesis and irregular lining of the lateral ventricles on CT-scan. A distinct X-linked mental retardation syndrome?
    Vles JS, Fryns JP, Folmer K, Boon P, Buttiens M, Grubben C, Janevski B.
    Genet Couns; 1990 Jul 30; 1(2):97-102. PubMed ID: 2081003
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  • 12. A new X-linked mental retardation syndrome.
    Homfray T, Holland T, Patton M.
    Clin Dysmorphol; 1995 Oct 30; 4(4):289-93. PubMed ID: 8574418
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  • 13. New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures.
    Pettigrew AL, Jackson LG, Ledbetter DH.
    Am J Med Genet; 1991 Oct 30; 38(2-3):200-7. PubMed ID: 2018058
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  • 14. Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.
    Gustavson KH, Holmgren G, Blomquist HK, Mikkelsen M, Nordenson I, Poulsen H, Tommerup N.
    Clin Genet; 1981 Feb 30; 19(2):101-10. PubMed ID: 7193540
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  • 15. Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome.
    Briault S, Odent S, Lucas J, Le Merrer M, Turleau C, Munnich A, Moraine C.
    Am J Med Genet; 1999 Sep 10; 86(2):112-4. PubMed ID: 10449643
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  • 16. Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?
    Tariverdian G, Froster-Iskenius U, Deuschl G, Wolff G.
    Am J Med Genet; 1991 Sep 10; 38(2-3):208-11. PubMed ID: 2018059
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  • 17. Updating the N syndrome: occurrence of lymphoid malignancy and possible association with an increased rate of chromosome breakage.
    Hess RO, Hafez GR, Meisner LF.
    Am J Med Genet Suppl; 1987 Sep 10; 3():383-8. PubMed ID: 3130873
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  • 20. Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndrome.
    Parloir C, Fryns JP, Deroover J, Lebas E, Goffaux P, van den Berghe H.
    Clin Genet; 1977 Nov 10; 12(5):263-6. PubMed ID: 589847
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