TY  - GEN
AU  - Boycott,Kym M
AU  - Beaulieu,Chandree
AU  - Puffenberger,Erik G
AU  - McLeod,D Ross
AU  - Parboosingh,Jillian S
AU  - Innes,A Micheil
TI  - A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population
SN  - 1552-4833
PY  - 2010///0830
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 16
KW  - genetics
KW  - Developmental Disabilities
KW  - Facies
KW  - Female
KW  - Genetic Markers
KW  - Humans
KW  - Pedigree
KW  - Population
KW  - Syndrome
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.33379
ER  -