Novel NSDHL gene variant for...

BMJ Case Reports 2020 / 11 Vol. 13; Iss. 11

Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome

Maceda, Ebner Bon Gatus, Kratz, Lisa E, Ramos, Veronica Marie E, Abacan, Mary Ann R
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Volume:
13
Journal:
BMJ Case Reports
DOI:
10.1136/bcr-2020-236859
Date:
November, 2020
File:
PDF, 393 KB
2020
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