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 *

244 related articles for article (PubMed ID: 12068376)

  • 21. 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]  

  • 22. 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]  

  • 23. [Update on the genetics of X-linked mental retardation].
    Bahi-Buisson N; Chelly J; des Portes V
    Rev Neurol (Paris); 2006 Oct; 162(10):952-63. PubMed ID: 17028563
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-inactivation patterns in carriers of X-linked myotubular myopathy.
    Kristiansen M; Knudsen GP; Tanner SM; McEntagart M; Jungbluth H; Muntoni F; Sewry C; Gallati S; Ørstavik KH; Wallgren-Pettersson C
    Neuromuscul Disord; 2003 Aug; 13(6):468-71. PubMed ID: 12899873
    [TBL] [Abstract][Full Text] [Related]  

  • 25. X chromosome inactivation pattern in female carriers of X linked hypophosphataemic rickets.
    Orstavik KH; Orstavik RE; Halse J; Knudtzon J
    J Med Genet; 1996 Aug; 33(8):700-3. PubMed ID: 8863165
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations.
    Woodward K; Kirtland K; Dlouhy S; Raskind W; Bird T; Malcolm S; Abeliovich D
    Eur J Hum Genet; 2000 Jun; 8(6):449-54. PubMed ID: 10878666
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients-Lessons from Wide Genome Analyses.
    Dardik R; Avishai E; Lalezari S; Barg AA; Levy-Mendelovich S; Budnik I; Barel O; Khavkin Y; Kenet G; Livnat T
    Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445777
    [TBL] [Abstract][Full Text] [Related]  

  • 29. X chromosome inactivation in carriers of Barth syndrome.
    Orstavik KH; Orstavik RE; Naumova AK; D'Adamo P; Gedeon A; Bolhuis PA; Barth PG; Toniolo D
    Am J Hum Genet; 1998 Nov; 63(5):1457-63. PubMed ID: 9792874
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR).
    Van Buggenhout GJ; Trommelen JC; Brunner HG; Hamel BC; Fryns J
    Ann Genet; 2001; 44(1):47-55. PubMed ID: 11334618
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.
    Lau AW; Brown CJ; Peñaherrera M; Langlois S; Kalousek DK; Robinson WP
    Am J Hum Genet; 1997 Dec; 61(6):1353-61. PubMed ID: 9399909
    [TBL] [Abstract][Full Text] [Related]  

  • 32. X-chromosome inactivation patterns in Korean women with idiopathic recurrent spontaneous abortion.
    Kim JW; Park SY; Kim YM; Kim JM; Han JY; Ryu HM
    J Korean Med Sci; 2004 Apr; 19(2):258-62. PubMed ID: 15082900
    [TBL] [Abstract][Full Text] [Related]  

  • 33. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.
    Gibbons RJ; Suthers GK; Wilkie AO; Buckle VJ; Higgs DR
    Am J Hum Genet; 1992 Nov; 51(5):1136-49. PubMed ID: 1415255
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2.
    Bar-David S; Lerer I; Sarfaty CK; Kohan ZG; Meiner V; Zlotogora J; Abeliovich D
    Am J Med Genet; 1996 Jul; 64(1):83-8. PubMed ID: 8826456
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.
    Arveiler B; Alembik Y; Hanauer A; Jacobs P; Tranebjaerg L; Mikkelsen M; Puissant H; Piet LL; Mandel JL
    Am J Med Genet; 1988; 30(1-2):473-83. PubMed ID: 3177465
    [TBL] [Abstract][Full Text] [Related]  

  • 36. X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status.
    Schmidt M; Du Sart D; Kalitsis P; Fraser N; Leversha M; Voullaire L; Foster D; Davies J; Hills L; Petrovic V
    Am J Med Genet; 1991; 38(2-3):411-5. PubMed ID: 1673316
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.
    Mason JA; Aung HT; Nandini A; Woods RG; Fairbairn DJ; Rowell JA; Young D; Susman RD; Brown SA; Hyland VJ; Robertson JD
    Mol Genet Genomic Med; 2018 May; 6(3):357-369. PubMed ID: 29490426
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.
    Martínez F; Martínez-Garay I; Oltra S; Moltó MD; Orellana C; Monfort S; Prieto F; Tejada I
    Am J Med Genet A; 2004 Dec; 131(2):174-8. PubMed ID: 15526294
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia.
    Abidi FE; Holloway L; Moore CA; Weaver DD; Simensen RJ; Stevenson RE; Rogers RC; Schwartz CE
    J Med Genet; 2008 Dec; 45(12):787-93. PubMed ID: 18697827
    [TBL] [Abstract][Full Text] [Related]  

  • 40. X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortium.
    des Portes V; Beldjord C; Chelly J; Hamel B; Kremer H; Smits A; van Bokhoven H; Ropers HH; Claes S; Fryns JP; Ronce N; Gendrot C; Toutain A; Raynaud M; Moraine C
    Am J Med Genet; 1999 Jul; 85(3):263-5. PubMed ID: 10398240
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.