(Q48906031)

16 February 2018

title

21-hydroxylase deficiency and Turner's syndrome: a reason for diminished endometrial receptivity (English)

1 reference

16 February 2018

author name string

Cohen MA

series ordinal

1

1 reference

16 February 2018

Sauer MV

series ordinal

2

1 reference

16 February 2018

Lindheim SR

series ordinal

3

1 reference

16 February 2018

language of work or name

English

0 references

publication date

1 November 1999

1 reference

16 February 2018

published in

Fertility and Sterility

1 reference

16 February 2018

volume

72

1 reference

16 February 2018

issue

5

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16 February 2018

page(s)

937-939

1 reference

16 February 2018

Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2899%2900378-7

Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2899%2900378-7

Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2899%2900378-7

Administration of progesterone before oocyte retrieval negatively affects the implantation rate.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2899%2900378-7

Patients with Turner's syndrome may have an inherent endometrial abnormality affecting receptivity in oocyte donation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2899%2900378-7

10.1016/S0015-0282(99)00378-7

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

1 reference

16 February 2018