(Q38294860)

1 September 2017

title

Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss (English)

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1 September 2017

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Uehara S

1

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1 September 2017

Hashiyada M

2

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1 September 2017

Sato K

3

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1 September 2017

Sato Y

4

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1 September 2017

Fujimori K

5

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1 September 2017

Okamura K

6

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1 September 2017

language of work or name

English

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publication date

1 November 2001

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1 September 2017

published in

Fertility and Sterility

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1 September 2017

volume

76

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1 September 2017

issue

5

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1 September 2017

page(s)

908-914

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Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 September 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0015-0282%2801%2902845-X

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X-chromosome inactivation in the human trophoblast of early pregnancy

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X chromosome inactivation patterns in 45,X/46,XX mosaics

7 January 2021

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Acquired skewing of X-chromosome inactivation patterns in myeloid cells of the elderly suggests stochastic clonal loss with age.

7 January 2021

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A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

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Fetal loss rates and their relation to pregnancy order

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IVF and embryo transfer--a therapeutic approach for unexplained recurrent miscarriages

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Sex Chromosome Genetics '99. The X chromosome and recurrent spontaneous abortion: the significance of transmanifesting carriers

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Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion

7 January 2021

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Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion

7 January 2021

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A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR.

7 January 2021

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Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family.

7 January 2021

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Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).

7 January 2021

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Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23.

7 January 2021

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Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28

7 January 2021

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A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

7 January 2021

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7 January 2021

Identifiers

DOI

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1 September 2017

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