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Doris K Wu

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Plos Genetics|March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndromeMariella Simon, Elodie M Richard, Xinjian Wang, et al.
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Showing results (41-50 of 42) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 42 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2026
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadismMaria Stamou, Miranda Tompkins, Hannah Bow, et al.
Plos Genetics|March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndromeMariella Simon, Elodie M Richard, Xinjian Wang, et al.
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