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Jessica Albert
Jessica Albert
National Institutes of Health
Genetics
Biology
Genetic testing
Snyder-Robinson syndrome
Internal medicine
5
Papers
27
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Minimal efficacy of nitisinone treatment in a novel mouse model of oculocutaneous albinism, type 3
2018
Investigative Ophthalmology & Visual Science
Ighovie F. Onojafe
Lucyanne H. Megan
Madeline G. Melch
Joseph O. Aderemi
Ramakrishna P. Alur
Mones Abu-Asab
Chi-Chao Chan
Isa Bernardini
Jessica Albert
Tiziana Cogliati
David R. Adams
Brian P. Brooks
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Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome
2015
Orphanet Journal of Rare Diseases
Jessica Albert
Nisan Bhattacharyya
Lynne A. Wolfe
William P. Bone
Valerie Maduro
John Accardi
David R. Adams
Charles E. Schwartz
Joy Norris
Tim Wood
Rachel I. Gafni
Michael T. Collins
Laura L. Tosi
Thomas C. Markello
William A. Gahl
Cornelius F. Boerkoel
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Citations (17)
Snyder-Robinson Syndrome
2013
Jessica Albert
Charles E. Schwartz
Cornelius F. Boerkoel
Roger E. Stevenson
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Citations (5)
Table 2. [SMS Pathogenic Variants Discussed in This GeneReview].
2013
Jessica Albert
Charles E. Schwartz
Cornelius F. Boerkoel
Roger E. Stevenson
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Table 1. [Summary of Molecular Genetic Testing Used in Snyder-Robinson Syndrome].
2013
Jessica Albert
Charles E. Schwartz
Cornelius F. Boerkoel
Roger E. Stevenson
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