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Michael Freemark

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The Journal of Clinical Endocrinology and Metabolism|December 16, 2004
Childhood obesityPhyllis W Speiser, Mary C J Rudolf, Henry Anhalt, et al.
American Journal of Human Genetics|January 31, 2017
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental DelayKelly Schoch, Linyan Meng, Szabolcs Szelinger, et al.
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Showing results (51-60 of 52) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 52 results.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2004
Childhood obesityPhyllis W Speiser, Mary C J Rudolf, Henry Anhalt, et al.
American Journal of Human Genetics|January 31, 2017
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental DelayKelly Schoch, Linyan Meng, Szabolcs Szelinger, et al.
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