Heterozygous deletions in MKRN3 cause central precocious...

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Heterozygous deletions in MKRN3 cause central precocious puberty without Prader-Willi Syndrome

Meader, Brooke N, Albano, Alessandro, Sekizkardes, Hilal, Delaney, Angela
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Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/clinem/dgaa331
Date:
June, 2020
File:
PDF, 702 KB
2020
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