Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.

Pebrel-Richard, Celine

Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay. [electronic resource] - American journal of medical genetics. Part A Nov 2014 - 2964-7 p. digital

Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't

1552-4833

10.1002/ajmg.a.36715 doi


Child, Preschool
Chromosome Duplication
Chromosomes, Human, Pair 7
Comparative Genomic Hybridization
Craniofacial Abnormalities--diagnosis
Facies
Humans
Language Development Disorders--diagnosis
Male
Phenotype
Syndrome