TY  - GEN
AU  - Stewart,Douglas R
AU  - Huang,Alina
AU  - Faravelli,Francesca
AU  - Anderlid,Britt-Marie
AU  - Medne,Livija
AU  - Ciprero,Karen
AU  - Kaur,Maninder
AU  - Rossi,Elena
AU  - Tenconi,Romano
AU  - Nordenskjöld,Magnus
AU  - Gripp,Karen W
AU  - Nicholson,Linda
AU  - Meschino,Wendy S
AU  - Capua,Esther
AU  - Quarrell,Oliver W J
AU  - Flint,Jonathon
AU  - Irons,Mira
AU  - Giampietro,Philip F
AU  - Schowalter,David B
AU  - Zaleski,Christina A
AU  - Malacarne,Michela
AU  - Zackai,Elaine H
AU  - Spinner,Nancy B
AU  - Krantz,Ian D
TI  - Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome
SN  - 1552-4825
PY  - 2005///0218
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 9
KW  - Cohort Studies
KW  - Cytogenetic Analysis
KW  - Female
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Microcephaly
KW  - Microsatellite Repeats
KW  - Polymorphism, Single Nucleotide
KW  - Syndrome
KW  - Telomere
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ajmg.a.30136
ER  -