TY  - GEN
AU  - POHL,D R
TI  - Pierre Robin syndrome
SN  - 0009-4129
PY  - 2002///0501
KW  - Child
KW  - Cyanosis
KW  - Facial Bones
KW  - abnormalities
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Infant, Newborn, Diseases
KW  - Laryngeal Diseases
KW  - Larynx
KW  - Pierre Robin Syndrome
N1  - Publication Type: Journal Article
ER  -