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Molecular Genetics & Genomic Medicine|February 14, 2022

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patientsJianbo Zhao, Guizhen Lyu, Changhong Ding, et al.

Pharmacogenomics and Personalized Medicine|April 28, 2025

Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier ScreeningPeng Lin, Huituan Liu, Jiwu Lou, et al.

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Showing results (31-40 of 32) with videos related to

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You have reached the last page of results.This site can display upto 32 results.

Molecular Genetics & Genomic Medicine|February 14, 2022

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patientsJianbo Zhao, Guizhen Lyu, Changhong Ding, et al.

Pharmacogenomics and Personalized Medicine|April 28, 2025

Novel SLC16A2 Frameshift Mutation as a Cause of Allan-Herndon-Dudley Syndrome and its Implications for Carrier ScreeningPeng Lin, Huituan Liu, Jiwu Lou, et al.

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