White‐Brown, A. M., Lemire, G., Ito, Y. A., Thornburg, O., Bain, J. M., & Dyment, D. A. (2021). A disease‐causing variant in HNRNPH2 inherited from an unaffected mother with skewed X‐inactivation. American Journal of Medical Genetics Part A, 188(2), 668–671. Portico. https://doi.org/10.1002/ajmg.a.62549
Subjects:
Mothers
(MeSH)
X Chromosome Inactivation
(MeSH)
Publication Type:
Article
Unique ID:
10.1002/ajmg.a.62549
PMID:
DOI:
Publication Date:
Data Source:
PubMed
Source Link: