TY  - GEN
AU  - Ferrante,E
AU  - Chessa,L
AU  - Bruni,L
AU  - Tozzi,M C
AU  - Lo Cuoco,A
TI  - [18p syndrome -- caused by 18/21 translocation]
SN  - 0026-4946
PY  - 1979///0925
KW  - Child
KW  - Chromosome Aberrations
KW  - Chromosome Deletion
KW  - Chromosomes, Human, 16-18
KW  - Chromosomes, Human, 21-22 and Y
KW  - Female
KW  - Humans
KW  - Infant, Newborn
KW  - Syndrome
KW  - Translocation, Genetic
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -