Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.1111/jog.15187
dc.identifier.other
WOS:000753285600001
dc.description.volume
dc.description.issue
Publisher
WILEY
DOI
10.1111/jog.15187