TY  - GEN
AU  - Pebrel-Richard,Celine
AU  - Rouzade,Charles
AU  - Kemeny,Stephan
AU  - Eymard-Pierre,Eleonore
AU  - Gay-Bellile,Mathilde
AU  - Gouas,Laetitia
AU  - Tchirkov,Andreï
AU  - Goumy,Carole
AU  - Vago,Philippe
TI  - Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay
SN  - 1552-4833
PY  - 2016///0516
KW  - Child, Preschool
KW  - Chromosome Duplication
KW  - Chromosomes, Human, Pair 7
KW  - Comparative Genomic Hybridization
KW  - Craniofacial Abnormalities
KW  - diagnosis
KW  - Facies
KW  - Humans
KW  - Language Development Disorders
KW  - Male
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.36715
ER  -