Autosomal translocation associated with premature ovarian failure

Burton KA, K A Burton, Van Ee CC, C C Van Ee, Purcell K, K Purcell, Winship I, I Winship, Shelling AN, A N Shelling
Journal of medical genetics · 2000 · vol. 37(5) , pp. E2 · doi:10.1136/jmg.37.5.e2 · PMID:10807701 · PMC1734579
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This paper reports an autosomal translocation associated with premature ovarian failure, without providing further details due to the absence of an abstract.

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MeSH descriptors

Primary Ovarian Insufficiency Translocation, Genetic Adult Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 2 Female Humans Karyotyping Pedigree Primary Ovarian Insufficiency Translocation, Genetic

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