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Paper Details

Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.
J Obstet Gynaecol Res
7
2022
Author NameAffiliation
Kaya BilguvarYale Center for Genome Analysis, Yale School of Medicine
Kaya BilguvarYale School of Medicine
Kaya BilguvarAcibadem University School of Medicine
Ahmet Okay CaglayanYale School of Medicine
Ahmet Okay CaglayanDokuz Eylul University
Ahmet Okay CaglayanInstitute of Health Sciences, Dokuz Eylul University
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Release 1.2