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Tashunka Taylor-Miller

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Clinical Genetics|January 30, 2024
Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 geneMarlène Malbos, Emma Wakeling, Thierry Gautier, et al.
American Journal of Human Genetics|August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.
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Showing results (11-20 of 12) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 12 results.
Clinical Genetics|January 30, 2024
Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 geneMarlène Malbos, Emma Wakeling, Thierry Gautier, et al.
American Journal of Human Genetics|August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.
Pageof 2