Treatment of the Mayer–Rokitansky–Küster–Hauser syndrome with autologous in vitro cultured vaginal tissue: descriptive study of long‐term results and patient outcomes
Author:
Affiliation:
1. Department of Gynecologica and Obstetrical Sciences and Urological Sciences Sapienza University of Rome Rome Italy
2. Department of Experimental Medicine Sapienza University of Rome Rome Italy
Publisher
Wiley
Subject
Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1471-0528.15477
Reference14 articles.
1. ACOG Committee Opinion No. 274: Nonsurgical Diagnosis and Management of Vaginal Agenesis
2. Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)
3. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
4. Haploinsufficiency of the HOXA Gene Cluster, in a Patient with Hand-Foot-Genital Syndrome, Velopharyngeal Insufficiency, and Persistent Patent Ductus Botalli
5. Atypical form of Mayer‐Rokitansky‐Küster‐Hauser syndrome;Schmid‐Tannwald I;Geburtshilfe Frauenheilkd,1977
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