Pregnancy Outcome in Recurrent Miscarriage Patients With Skewed X Chromosome Inactivation

[1]  H. Willard,et al.  Autosomal Dominant Mutations Affecting X Inactivation Choice in the Mouse , 2002, Science.

[2]  K. Okamura,et al.  Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss. , 2001, Fertility and sterility.

[3]  E. Hoffman,et al.  A novel X chromosome-linked genetic cause of recurrent spontaneous abortion. , 2001, American Journal of Obstetrics and Gynecology.

[4]  N. Lévy,et al.  Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome withoutMECP2 mutation: implications for the disease , 2001, Journal of medical genetics.

[5]  Carolyn J. Brown,et al.  Skewed X Inactivation and Recurrent Spontaneous Abortion , 2001, Seminars in reproductive medicine.

[6]  I. Veyver Skewed X inactivation in X-linked disorders. , 2001 .

[7]  A. Sharp,et al.  Age- and tissue-specific variation of X chromosome inactivation ratios in normal women , 2000, Human Genetics.

[8]  C. Ober,et al.  A null mutation in HLA-G is not associated with preeclampsia or intrauterine growth retardation. , 2000, Journal of reproductive immunology.

[9]  Carolyn J. Brown,et al.  Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion. , 1999, American journal of human genetics.

[10]  C. Ober,et al.  Mononuclear-cell immunisation in prevention of recurrent miscarriages: a randomised trial , 1999, The Lancet.

[11]  E. Hoffman,et al.  Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion. , 1999, American journal of human genetics.

[12]  D. Lev,et al.  Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother , 1999, Human Genetics.

[13]  H. Tenenhouse,et al.  X-linked hypophosphataemia: a homologous disorder in humans and mice. , 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[14]  M. Leppert,et al.  Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human , 1998, European Journal of Human Genetics.

[15]  Carolyn J. Brown,et al.  Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. , 1997, American journal of human genetics.

[16]  Robert M. Plenge,et al.  A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation , 1997, Nature Genetics.

[17]  U. Surti,et al.  Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28. , 1997, American journal of human genetics.

[18]  L. Tranebjaerg,et al.  Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome. , 1996, American journal of medical genetics.

[19]  J. Belmont Genetic control of X inactivation and processes leading to X-inactivation skewing. , 1996, American journal of human genetics.

[20]  M. Varner,et al.  Recurrent pregnancy loss. , 1994, Current opinion in obstetrics & gynecology.

[21]  Clarice R. Weinberg,et al.  Incidence of early loss of pregnancy. , 1988, The New England journal of medicine.

[22]  M. Lyon Possible mechanisms of X chromosome inactivation. , 1971, Nature: New biology.

[23]  M. Lyon Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.

[24]  I. B. Van den Veyver Skewed X inactivation in X-linked disorders. , 2001, Seminars in reproductive medicine.

[25]  W. A. Hogge,et al.  X Chromosome Defects as an Etiology of Recurrent Spontaneous Abortion , 2000, Seminars in reproductive medicine.

[26]  H. Zoghbi,et al.  Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. , 1992, American journal of human genetics.

[27]  B. Cattanach Control of chromosome inactivation. , 1975, Annual review of genetics.