TY  - GEN
AU  - Gorski,J L
AU  - Cox,B A
AU  - Kyine,M
AU  - Uhlmann,W
AU  - Glover,T W
TI  - Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)
SN  - 0148-7299
PY  - 1989///0630
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Chromosome Aberrations
KW  - pathology
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 2
KW  - Facial Muscles
KW  - physiopathology
KW  - Growth Disorders
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Male
KW  - Muscle Hypotonia
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ajmg.1320320315
ER  -