TY  - GEN
AU  - Luciani,J J
AU  - de Mas,P
AU  - Depetris,D
AU  - Mignon-Ravix,C
AU  - Bottani,A
AU  - Prieur,M
AU  - Jonveaux,P
AU  - Philippe,A
AU  - Bourrouillou,G
AU  - de Martinville,B
AU  - Delobel,B
AU  - Vallee,L
AU  - Croquette,M-F
AU  - Mattei,M-G
TI  - Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations
SN  - 1468-6244
PY  - 2003///0930
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - genetics
KW  - Chromosomes, Human, Pair 20
KW  - Developmental Disabilities
KW  - pathology
KW  - Female
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Male
KW  - Mental Disorders
KW  - Monosomy
KW  - Ring Chromosomes
KW  - Telomere
KW  - Translocation, Genetic
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmg.40.9.690
ER  -