BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (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; 85(3):236-42. PubMed ID: 10398235
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 85(3):230-5. PubMed ID: 10398234
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):223-9. PubMed ID: 10398233
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian family.
    Russo S; Cogliati F; Cavalleri F; Cassitto MG; Giglioli R; Toniolo D; Casari G; Larizza L
    Am J Med Genet; 2000 Oct; 94(5):376-82. PubMed ID: 11050621
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):243-8. PubMed ID: 10398236
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 37(9):663-8. PubMed ID: 10978355
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):271-5. PubMed ID: 10398242
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):255-62. PubMed ID: 10398239
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 103(1):1-8. PubMed ID: 11562927
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 34(7):529-34. PubMed ID: 9222958
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
    Holinski-Feder E; Chahrockh-Zadeh S; Rittinger O; Jedele KB; Gasteiger M; Lenski C; Murken J; Golla A
    Am J Med Genet; 1999 Sep; 86(2):102-6. PubMed ID: 10449641
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 62(5):1092-101. PubMed ID: 9545405
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 102(2):200-4. PubMed ID: 11477616
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 124A(2):136-41. PubMed ID: 14699611
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
    Shrimpton AE; Braddock BR; Hoo JJ
    Am J Med Genet; 2000 May; 92(2):155-6. PubMed ID: 10797443
    [No Abstract]   [Full Text] [Related]  

  • 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; 88(2):228-30. PubMed ID: 1757098
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):216-20. PubMed ID: 10398231
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 85(3):266-70. PubMed ID: 10398241
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 100(1):62-5. PubMed ID: 11337751
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 30(1-2):485-91. PubMed ID: 3177466
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.