TY  - GEN
AU  - Herman,G E
AU  - Greenberg,F
AU  - Ledbetter,D H
TI  - Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)
SN  - 0148-7299
PY  - 1988///0831
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - Goldenhar Syndrome
KW  - Humans
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Male
KW  - Mandibulofacial Dysostosis
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.1320290423
ER  -