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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Elizabeth C Engle

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Genetics in Medicine Open|July 15, 2025

Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.

Cell|January 16, 2010

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.

Medrxiv : the Preprint Server for Health Sciences|May 19, 2025

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson SyndromeKimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M Nodelman, et al.

Nature Genetics|June 29, 2023

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.

Medrxiv : the Preprint Server for Health Sciences|July 3, 2026

Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.

Pageof 13

Search research articles

Showing results (121-130 of 125) with videos related to

Sort By:

Pageof 13

You have reached the last page of results.This site can display upto 125 results.

Genetics in Medicine Open|July 15, 2025

Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.

Cell|January 16, 2010

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.

Medrxiv : the Preprint Server for Health Sciences|May 19, 2025

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson SyndromeKimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M Nodelman, et al.

Nature Genetics|June 29, 2023

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.

Medrxiv : the Preprint Server for Health Sciences|July 3, 2026

Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.

Pageof 13