A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. (Q47303227)

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scientific article published on 12 December 2017
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A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.
scientific article published on 12 December 2017

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    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency (English)

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