DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Kausar M, Chew EGY, Ullah H. et al.
A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family.
Front Genet 2019;
10: 144
We do not assume any responsibility for the contents of the web pages of other providers.