Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype.

Hoppman-Chaney, N

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype. [electronic resource] - Clinical genetics Apr 2013 - 345-51 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1399-0004

10.1111/j.1399-0004.2012.01925.x doi


Adolescent
Adult
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 15
Female
Gene Deletion
Genotype
Homozygote
Humans
Infant
Intellectual Disability--genetics
Male
Middle Aged
Pedigree
Phenotype
Syndrome
Young Adult
alpha7 Nicotinic Acetylcholine Receptor--genetics