Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males.

Name: Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males.
Author: Mullegama, Sureni V

Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. — المؤلف: Mullegama, Sureni V — Molecular genetics & genomic medicine 20190411

المؤلف: Mullegama, Sureni V
النشر: Molecular genetics & genomic medicine 20190411
الوصف: e00501 p.
الموضوعات: Antigens, Nuclear؛ Cell Cycle Proteins؛ Child, Preschool؛ Developmental Disabilities؛ Genetic Diseases, X-Linked؛ Growth Disorders؛ Humans؛ Male