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Anna C Thomas

Showing results (21-30 of 24) with videos related to

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The Journal of Investigative Dermatology|August 12, 2006
ABCA12 is the major harlequin ichthyosis geneAnna C Thomas, Tom Cullup, Elizabeth E Norgett, et al.
The Journal of Investigative Dermatology|January 19, 2016
Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal MelanocytosisAnna C Thomas, Zhiqiang Zeng, Jean-Baptiste Rivière, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2021
Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotypeSatyamaanasa Polubothu, Davide Zecchin, Lara Al-Olabi, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
The Journal of Investigative Dermatology|August 12, 2006
ABCA12 is the major harlequin ichthyosis geneAnna C Thomas, Tom Cullup, Elizabeth E Norgett, et al.
The Journal of Investigative Dermatology|January 19, 2016
Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal MelanocytosisAnna C Thomas, Zhiqiang Zeng, Jean-Baptiste Rivière, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2021
Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotypeSatyamaanasa Polubothu, Davide Zecchin, Lara Al-Olabi, et al.
Pageof 3