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Journal Abstract Search

194 related items for PubMed ID: 10398235

  • 1. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.
    Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE.
    Am J Med Genet; 1999 Jul 30; 85(3):236-42. PubMed ID: 10398235
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  • 3. X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.
    Abidi F, Hall BD, Cadle RG, Feldman GL, Lubs HA, Ouzts LV, Arena JF, Stevenson RE, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):223-9. PubMed ID: 10398233
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  • 5. XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28.
    Lubs H, Abidi F, Bier JA, Abuelo D, Ouzts L, Voeller K, Fennell E, Stevenson RE, Schwartz CE, Arena F.
    Am J Med Genet; 1999 Jul 30; 85(3):243-8. PubMed ID: 10398236
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  • 6. A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.
    Cabezas DA, Slaugh R, Abidi F, Arena JF, Stevenson RE, Schwartz CE, Lubs HA.
    J Med Genet; 2000 Sep 30; 37(9):663-8. PubMed ID: 10978355
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  • 7. Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22.
    Häne B, Stevenson RE, Arena JF, Lubs HA, Simensen RJ, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):271-5. PubMed ID: 10398242
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  • 8. X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23.
    Chudley AE, Tackels DC, Lubs HA, Arena JF, Stoeber WP, Kovnats S, Stevenson RE, Schwartz CE.
    Am J Med Genet; 1999 Jul 30; 85(3):255-62. PubMed ID: 10398239
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  • 9. Novel X-linked mental retardation syndrome with short stature maps to Xq24.
    Vitale E, Specchia C, Devoto M, Angius A, Rong S, Rocchi M, Schwalb M, Demelas L, Paglietti D, Manca S, Mastropaolo C, Serra G.
    Am J Med Genet; 2001 Sep 15; 103(1):1-8. PubMed ID: 11562927
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  • 10. A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.
    Pai GS, Hane B, Joseph M, Nelson R, Hammond LS, Arena JF, Lubs HA, Stevenson RE, Schwartz CE.
    J Med Genet; 1997 Jul 15; 34(7):529-34. PubMed ID: 9222958
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  • 12. Renpenning syndrome maps to Xp11.
    Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE.
    Am J Hum Genet; 1998 May 15; 62(5):1092-101. PubMed ID: 9545405
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  • 13. Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.
    Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F.
    Am J Med Genet; 2001 Aug 01; 102(2):200-4. PubMed ID: 11477616
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  • 14. The 10q24-linked split hand/split foot syndrome (SHFM3): narrowing of the critical region and confirmation of the clinical phenotype.
    Roscioli T, Taylor PJ, Bohlken A, Donald JA, Masel J, Glass IA, Buckley MF.
    Am J Med Genet A; 2004 Jan 15; 124A(2):136-41. PubMed ID: 14699611
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  • 16. Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.
    Biancalana V, Le Marec B, Odent S, van den Hurk JA, Hanauer A.
    Hum Genet; 1991 Dec 15; 88(2):228-30. PubMed ID: 1757098
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  • 17. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
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  • 18. Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2.
    Carpenter NJ, Brown WT, Qu Y, Keenan KL.
    Am J Med Genet; 1999 Jul 30; 85(3):266-70. PubMed ID: 10398241
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  • 19. Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
    Ahmad W, Noci S, Faiyaz ul Haque M, Sarno T, Aridon P, Ahmad MM, Amin-Ud-Din M, Rafiq MA, ul Haque S, De Fusco M, Ballabio A, Franco B, Casari G.
    Am J Med Genet; 2001 Apr 15; 100(1):62-5. PubMed ID: 11337751
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  • 20. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.
    Suthers GK, Turner G, Mulley JC.
    Am J Med Genet; 1988 Apr 15; 30(1-2):485-91. PubMed ID: 3177466
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