TY  - GEN
AU  - Stoll,C
AU  - Medeiros,P
AU  - Pécheur,H
AU  - Schnebelen,A
TI  - De novo trisomy 22 due to an extra 22Q-chromosome
SN  - 0003-3995
PY  - 1998///0429
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 22
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - genetics
KW  - Karyotyping
KW  - Male
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article
ER  -