These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 7581391)

  • 1. Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.
    May M; Colleaux L; Murgia A; Aylsworth A; Nussbaum R; Fontes M; Schwartz C
    Hum Mol Genet; 1995 Aug; 4(8):1465-6. PubMed ID: 7581391
    [No Abstract]   [Full Text] [Related]  

  • 2. Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.
    Cremers FP; van de Pol DJ; Diergaarde PJ; Wieringa B; Nussbaum RL; Schwartz M; Ropers HH
    Genomics; 1989 Jan; 4(1):41-6. PubMed ID: 2914708
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
    Merry DE; Lesko JG; Sosnoski DM; Lewis RA; Lubinsky M; Trask B; van den Engh G; Collins FS; Nussbaum RL
    Am J Hum Genet; 1989 Oct; 45(4):530-40. PubMed ID: 2491012
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation.
    van der Maarel SM; Scholten IH; Maat-Kievit JA; Huber I; de Kok YJ; de Wijs I; van de Pol TJ; van Bokhoven H; den Dunnen JT; van Ommen GJ
    Eur J Hum Genet; 1995; 3(4):207-18. PubMed ID: 8528669
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.
    Rosenberg T; Niebuhr E; Yang HM; Parving A; Schwartz M
    Ophthalmic Paediatr Genet; 1987 Nov; 8(3):139-43. PubMed ID: 3438052
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DXS26 (HU16) is located in Xq21.1.
    Sankila EM; Bruns GA; Schwartz M; Nikoskelainen E; Niebuhr E; Hodgson SV; Wright AF; de la Chapelle A
    Hum Genet; 1990 Jun; 85(1):117-20. PubMed ID: 2162804
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.
    Bach I; Robinson D; Thomas N; Ropers HH; Cremers FP
    Hum Genet; 1992 Aug; 89(6):620-4. PubMed ID: 1511979
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation.
    Migeon BR; Stetten G; Tuck-Muller C; Axelman J; Jani M; Dungy D
    Somat Cell Mol Genet; 1995 Mar; 21(2):113-20. PubMed ID: 7570183
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage studies and deletion screening in choroideremia.
    Wright AF; Nussbaum RL; Bhattacharya SS; Jay M; Lesko JG; Evans HJ; Jay B
    J Med Genet; 1990 Aug; 27(8):496-8. PubMed ID: 1976814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MRX8: an X-linked mental retardation condition with linkage to Xq21.
    Schwartz CE; May M; Huang T; Ledbetter D; Anderson G; Barker DF; Lubs HA; Arena F; Stevenson RE
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):467-74. PubMed ID: 1605227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.
    Nussbaum RL; Lesko JG; Lewis RA; Ledbetter SA; Ledbetter DH
    Proc Natl Acad Sci U S A; 1987 Sep; 84(18):6521-5. PubMed ID: 3476958
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel ribosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardation.
    Yntema HG; van den Helm B; Kissing J; van Duijnhoven G; Poppelaars F; Chelly J; Moraine C; Fryns JP; Hamel BC; Heilbronner H; Pander HJ; Brunner HG; Ropers HH; Cremers FP; van Bokhoven H
    Genomics; 1999 Dec; 62(3):332-43. PubMed ID: 10644430
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient.
    Liang S; Jiang N; Li S; Jiang X; Yu D
    Mol Cytogenet; 2017; 10():23. PubMed ID: 28630650
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB; Michels VV; Schaid DJ; Schowalter KV; Thibodeau SN
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):436-42. PubMed ID: 1605223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardation.
    Billuart P; Vinet MC; des Portes V; Llense S; Richard L; Moutard ML; Recan D; Brüls T; Bienvenu T; Kahn A; Beldjord C; Chelly J
    Hum Mol Genet; 1996 Jul; 5(7):977-9. PubMed ID: 8817333
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands.
    Colleaux L; May M; Belougne J; Lepaslier D; Schwartz C; Fontes M
    J Med Genet; 1996 May; 33(5):353-7. PubMed ID: 8733041
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic linkage analysis places locus DXS250 between locus DXYS1 and locus DXS3 in Xq21.3.
    Epting S; Schwartz C
    Cytogenet Cell Genet; 1992; 60(2):112-3. PubMed ID: 1611908
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).
    Bach I; Brunner HG; Beighton P; Ruvalcaba RH; Reardon W; Pembrey ME; van der Velde-Visser SD; Bruns GA; Cremers CW; Cremers FP
    Am J Hum Genet; 1992 Jul; 51(1):38-44. PubMed ID: 1609803
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.