Autosomal chromosome microdeletions in three adolescent girls with premature ovarian insufficiency: a case report

Background. Premature ovarian insufficiency (POI) in the pediatric age group is most commonly related to X chromosome abnormalities such as Turner syndrome. Autosomal chromosome microdeletions in ovarian failure are relatively rare. The present study identified new autosomal deletions in thre...

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מידע ביבליוגרפי

Principais autores:	Ke Yuan, Minfei He, Yanlan Fang, Jianfang Zhu, Li Liang, Chunlin Wang
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	Hacettepe University Institute of Child Health 2022-08-01
סדרה:	The Turkish Journal of Pediatrics
נושאים:	autosomal chromosomal abnormalities chromosome karyotype chromosome microarray analysis premature ovarian insufficiency
גישה מקוונת:	https://turkjpediatr.org/article/view/202
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