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Climacteric Volume 14, 2011 - Issue 2
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Case Report

Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism

K. Gersak Division of Medical Genetics, Department of Obstetrics and Gynaecology, University Medical Centre Ljubljana
,
D. Franic *Outpatient Clinic of Obstetrics & Gynecology Dr. Franic, Rogaska Slatina
,
A. Veble Division of Medical Genetics, Department of Obstetrics and Gynaecology, University Medical Centre Ljubljana
,
I. Zupanic Pajnic Institute of Forensic Medicine, Faculty of Medicine, University of Ljubljana, Slovenia
,
N. Teran Division of Medical Genetics, Department of Obstetrics and Gynaecology, University Medical Centre Ljubljana
&
K. Writzl Division of Medical Genetics, Department of Obstetrics and Gynaecology, University Medical Centre Ljubljana
Pages 289-293 | Received 13 Jan 2010, Accepted 25 Apr 2010, Published online: 24 Jun 2010

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Sengul Tural, Akın Tekcan, Nurten Kara, Mehmet Elbistan, Davut Güven & Haydar Ali Tasdemir. (2015) FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X. Gynecological Endocrinology 31:3, pages 191-195.
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Articles from other publishers (1)

K. Gersak & A. Veble. (2011) Low-level X chromosome mosaicism in women with sporadic premature ovarian failure. Reproductive BioMedicine Online 22:4, pages 399-403.
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