Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation-Reference-Cited by-同舟云学术

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Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation

Published:2012-02-14 Issue:3 Volume:82 Page:295-296
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Ye Y,Cong P,Yu P,Qi M,Jin F

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01847.x/fullpdf

Reference6 articles.

1. Androgen insensitivity syndrome: clinical features and molecular defects.;Galani;Hormones (Athens),2008

2. Molecular basis of androgen insensitivity.;Brinkmann;Mol Cell Endocrinol,2001

3. Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene.;Vilchis;J Hum Genet,2003

4. ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008.;Harper;Hum Reprod,2010

5. When is old too old for preimplantation genetic diagnosis for reciprocal translocations?;Xanthopoulou;Prenat Diagn,2011

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Androgen Insensitivity Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

2. Androgen Insensitivity Syndrome;Atlas of Genetic Diagnosis and Counseling;2015

3. Gender Eugenics? The Ethics of PGD for Intersex Conditions;The American Journal of Bioethics;2013-10

4. FSH in vitro versus LH in vivo: similar genomic effects on the cumulus;Journal of Ovarian Research;2013-09-25

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