TY  - GEN
AU  - Fernandez,Thomas V
AU  - García-González,I J
AU  - Mason,Christopher E
AU  - Hernández-Zaragoza,G
AU  - Ledezma-Rodríguez,V C
AU  - Anguiano-Alvarez,V M
AU  - E'Vega,R
AU  - Gutiérrez-Angulo,M
AU  - Maya,M L
AU  - García-Bejarano,H E
AU  - González-Cruz,M
AU  - Barrios,S
AU  - Atorga,R
AU  - López-Cardona,M G
AU  - Armendariz-Borunda,J
AU  - State,Matthew W
AU  - Dávalos,Nory O
TI  - Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
SN  - 1552-4833
PY  - 2008///1209
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - genetics
KW  - Chromosomes, Human, Pair 13
KW  - Chromosomes, Human, Pair 3
KW  - Comparative Genomic Hybridization
KW  - Craniofacial Abnormalities
KW  - Developmental Disabilities
KW  - Female
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Karyotyping
KW  - Limb Deformities, Congenital
KW  - Male
KW  - Phenotype
KW  - Syndrome
KW  - Translocation, Genetic
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1002/ajmg.a.32533
ER  -