200 related articles for article (PubMed ID: 9887372)
21. 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]
22. Transmission ratio distortion in families from the Framingham Heart Study.
Paterson AD; Sun L; Liu XQ;
BMC Genet; 2003 Dec; 4 Suppl 1(Suppl 1):S48. PubMed ID: 14975116
[TBL] [Abstract][Full Text] [Related]
23. The history of X-chromosome inactivation and relation of recent findings to understanding of human X-linked conditions.
Lyon MF
Turk J Pediatr; 1995; 37(2):125-40. PubMed ID: 7597763
[TBL] [Abstract][Full Text] [Related]
24. Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
Hendriks RW; Chen ZY; Hinds H; Schuurman RK; Craig IW
Immunodeficiency; 1993; 4(1-4):209-11. PubMed ID: 8167702
[TBL] [Abstract][Full Text] [Related]
25. A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.
Lanasa MC; Hogge WA; Kubik CJ; Ness RB; Harger J; Nagel T; Prosen T; Markovic N; Hoffman EP
Am J Obstet Gynecol; 2001 Sep; 185(3):563-8. PubMed ID: 11568778
[TBL] [Abstract][Full Text] [Related]
26. A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease.
Rosenberg C; Wouters CH; Szuhai K; Dorland R; Pearson P; Poll-The BT; Colombijn RM; Breuning M; Lindhout D
Eur J Hum Genet; 2001 Mar; 9(3):171-7. PubMed ID: 11313755
[TBL] [Abstract][Full Text] [Related]
27. Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus.
Cooper P; Keer JT; McCabe VM; Hamvas RM; Brown SD; Rastan S; Brockdorff N
Genomics; 1993 Mar; 15(3):570-5. PubMed ID: 8468051
[TBL] [Abstract][Full Text] [Related]
28. A novel expression based approach for assessing the inactivation status of human X-linked genes.
Benjamin D; Van Bakel I; Craig IW
Eur J Hum Genet; 2000 Feb; 8(2):103-8. PubMed ID: 10757641
[TBL] [Abstract][Full Text] [Related]
29. Human X inactivation center induces random X chromosome inactivation in male transgenic mice.
Migeon BR; Kazi E; Haisley-Royster C; Hu J; Reeves R; Call L; Lawler A; Moore CS; Morrison H; Jeppesen P
Genomics; 1999 Jul; 59(2):113-21. PubMed ID: 10409422
[TBL] [Abstract][Full Text] [Related]
30. Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation.
Sharp A; Robinson DO; Jacobs P
Hum Genet; 2001 Sep; 109(3):295-302. PubMed ID: 11702210
[TBL] [Abstract][Full Text] [Related]
31. A likelihood approach for quantitative-trait-locus mapping with selected pedigrees.
Wang K
Biometrics; 2005 Jun; 61(2):465-73. PubMed ID: 16011693
[TBL] [Abstract][Full Text] [Related]
32. Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene.
Kaplan Y; Vargel I; Kansu T; Akin B; Rohmann E; Kamaci S; Uz E; Ozcelik T; Wollnik B; Akarsu NA
Br J Ophthalmol; 2008 Jan; 92(1):135-41. PubMed ID: 17962394
[TBL] [Abstract][Full Text] [Related]
33. Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
Fearon ER; Winkelstein JA; Civin CI; Pardoll DM; Vogelstein B
N Engl J Med; 1987 Feb; 316(8):427-31. PubMed ID: 2880293
[TBL] [Abstract][Full Text] [Related]
34. Tsix, a gene antisense to Xist at the X-inactivation centre.
Lee JT; Davidow LS; Warshawsky D
Nat Genet; 1999 Apr; 21(4):400-4. PubMed ID: 10192391
[TBL] [Abstract][Full Text] [Related]
35. [X chromosome inactivation--a biological phenomenon of clinical significance for women].
Orstavik KH
Tidsskr Nor Laegeforen; 1999 Mar; 119(7):972-5. PubMed ID: 10210959
[TBL] [Abstract][Full Text] [Related]
36. Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family.
Köker MY; Sanal O; de Boer M; Tezcan I; Metin A; Tan C; Ersoy F; Roos D
Eur J Clin Invest; 2006 Apr; 36(4):257-64. PubMed ID: 16620288
[TBL] [Abstract][Full Text] [Related]
37. X chromosome inactivation revealed by the X-linked lacZ transgene activity in periimplantation mouse embryos.
Sugimoto M; Tan SS; Takagi N
Int J Dev Biol; 2000 Feb; 44(2):177-82. PubMed ID: 10794075
[TBL] [Abstract][Full Text] [Related]
38. [Influence of the X-chromosome on finger dermatoglyphic features in the Ukrainian population of Podolye].
Gal'perina ZZ; Kogan BI
Genetika; 1989 Apr; 25(4):720-6. PubMed ID: 2759445
[TBL] [Abstract][Full Text] [Related]
39. Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.
Gelernter J; Panhuysen C; Weiss R; Brady K; Poling J; Krauthammer M; Farrer L; Kranzler HR
Biol Psychiatry; 2007 Jan; 61(1):119-26. PubMed ID: 17081504
[TBL] [Abstract][Full Text] [Related]
40. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
Sutton BS; Langefeld CD; Campbell JK; Haffner SM; Norris JM; Scherzinger AL; Wagenknecht LE; Bowden DW
Int J Obes (Lond); 2006 Sep; 30(9):1433-41. PubMed ID: 16520807
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
