Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance.

Name: Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance.
Author: Woodward, Karen J

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance. — المؤلف: Woodward, Karen J — Molecular genetics & genomic medicine 20190411

المؤلف: Woodward, Karen J
النشر: Molecular genetics & genomic medicine 20190411
الوصف: e00507 p.
الموضوعات: Abnormalities, Multiple؛ Adolescent؛ Adult؛ Autism Spectrum Disorder؛ Child؛ Child, Preschool؛ Chromosome Duplication؛ Chromosomes, Human, Pair 22