TY  - GEN
AU  - Freitas,Érika L
AU  - Gribble,Susan M
AU  - Simioni,Milena
AU  - Vieira,Társis P
AU  - Silva-Grecco,Roseane L
AU  - Balarin,Marly A S
AU  - Prigmore,Elena
AU  - Krepischi-Santos,Ana C
AU  - Rosenberg,Carla
AU  - Szuhai,Karoly
AU  - van Haeringen,Arie
AU  - Carter,Nigel P
AU  - Gil-da-Silva-Lopes,Vera Lúcia
TI  - Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization
SN  - 1552-4833
PY  - 2012///0209
KW  - Abnormal Karyotype
KW  - Adolescent
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 20
KW  - genetics
KW  - Chromosomes, Human, Pair 9
KW  - Comparative Genomic Hybridization
KW  - methods
KW  - DNA Copy Number Variations
KW  - Developmental Disabilities
KW  - Forkhead Transcription Factors
KW  - Genome, Human
KW  - Guanine Nucleotide Exchange Factors
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Inheritance Patterns
KW  - Intellectual Disability
KW  - Male
KW  - Metaphase
KW  - Physical Examination
KW  - Trisomy
KW  - diagnosis
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.34168
ER  -