Detection of de novo genetic variants in Mayer–Rokitansky–Küster–Hauser syndrome by whole genome sequencing-Reference-Cited by-同舟云学术

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Detection of de novo genetic variants in Mayer–Rokitansky–Küster–Hauser syndrome by whole genome sequencing

Published:2019-10 Issue: Volume:4 Page:100089
ISSN:2590-1613
Container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology: X
language:en
Short-container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology: X

Author:

Pan Hong-xin^ORCID,Luo Guang-nan,Wan Sheng-qing,Qin Cheng-lu,Tang Jie,Zhang Meng,Du Min,Xu Ke-ke,Shi Jin-qiu

Funder

Health and Family Planning Commission of Guangdong Province

Shenzhen Healthcare Research Project

Sanming Project of Medicine in Shenzhen

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference40 articles.

1. Congenital anomalies of the Mullerian system;Golan;Fertil Steril,1989

2. Mullerian agenesis: etiology, diagnosis, and management;Folch;Obstet Gynecol Surv,2000

3. Phenotypic and clinical aspects of Mayer-Rokitansky-Kuster-Hauser syndrome in a Chinese population: an analysis of 594 patients;Pan;Fertil Steril,2016

4. Mutation screening of HOXA7 and HOXA9 genes in Chinese women with Mullerian duct abnormalities;Chen;Reprod Biomed Online,2014

5. Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina);Burel;J Negat Results Biomed,2006

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1. Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications;Frontiers in Endocrinology;2024-04-18

2. Molecular Basis of Müllerian Agenesis Causing Congenital Uterine Factor Infertility—A Systematic Review;International Journal of Molecular Sciences;2023-12-21

3. Recurrent human 16p11.2 microdeletions in type I Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome patients in Chinese Han population;Molecular Genetics & Genomic Medicine;2023-10-03

4. Genome Sequencing and Transcriptome Profiling in Twins Discordant for Mayer-Rokitansky-Küster-Hauser Syndrome;Journal of Clinical Medicine;2022-09-23

5. Identification of Genetic Causes in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Systematic Review of the Literature;Children;2022-06-27

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