Spectrum of Type I and Type II Syndromes and Associated Malformations in Chinese Patients with Mayer-Rokitansky-Küster-Hauser Syndrome: A Retrospective Analysis of 274 Cases-Reference-Cited by-同舟云学术

Spectrum of Type I and Type II Syndromes and Associated Malformations in Chinese Patients with Mayer-Rokitansky-Küster-Hauser Syndrome: A Retrospective Analysis of 274 Cases

Published:2019-06 Issue:3 Volume:32 Page:284-287
ISSN:1083-3188
Container-title:Journal of Pediatric and Adolescent Gynecology
language:en
Short-container-title:Journal of Pediatric and Adolescent Gynecology

Author:

Deng Shan,He Yonglan,Chen Na,Zhu Lan

Funder

National Science and Technology

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,General Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Mayer-Rokitansky-Kuster-Hauser syndrome: a review;Londra;Int J Womens Health,2015

2. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: a historical perspective;Patnaik;Gene,2015

3. Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging;Oppelt;Hum Reprod,2006

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

5. Mayer-Rokitansky-Kuster-Hauser syndrome and associated malformations: are they as common as we think?;Petrozza;Fertil Steril,2016

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5. 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