Based on a cohort of 52,879 microarrays, recurrent...

European Journal of Medical Genetics 2020 / 10 Vol. 63; Iss. 10

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1–8 does not cause Beals syndrome

Maya, Idit, Kahana, Sarit, Agmon-Fishman, Ifaat, Klein, Cochava, Matar, Reut, Berger, Racheli, Shohat, Mordechai, Basel-Salmon, Lina, Sharony, Reuven, Sagi-Dain, Lena
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
63
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2020.104008
Date:
October, 2020
File:
PDF, 1.46 MB
2020
Conversion to is in progress
Conversion to is failed