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. 2016 Sep 6;9(1):54. doi: 10.1186/s13048-016-0263-6

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Partial sequencing results of genetic variations in the patient for the FSHR gene. a Forward sequences in the patient. The arrow indicates the heterozygous variation c.-29G > A of 5′-UTR. b Forward sequences in the patient. The arrow indicates the heterozygous variation c.299 + 33C > T of intron 3. c Forward sequences in the patient. The arrow indicates the heterozygous variation c.919G > A (p.Ala307Thr) of exon 10. d Forward sequences in the patient. The arrow indicates the heterozygous variation c.2039G > A (p.Ser680Asn) of exon 10