Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

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Title:	Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease
Author(s):	Jolly, Angad; Bayram, Yavuz; Turan, Serap; Aycan, Zehra; Tos, Tulay; Abali, Zehra Yavas; Rinne, T.K. ; Posey, J.E.; Lupski, James R.
Publication year:	2019
Source:	Journal of Clinical Endocrinology and Metabolism, vol. 104, iss. 8, (2019), pp. 3049-3067
ISSN:	0021-972X
DOI:	https://doi.org/10.1210/jc.2019-00248
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/207316
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Subject:	All institutes and research themes of the Radboud University Medical Center Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
Organization:	Human Genetics
Journal title:	Journal of Clinical Endocrinology and Metabolism
Volume:	vol. 104
Issue:	iss. 8
Page start:	p. 3049
Page end:	p. 3067