TY  - GEN
AU  - Al-Kateb,Hussam
AU  - Hahn,Amanda
AU  - Gastier-Foster,Julie M
AU  - Jeng,Linda
AU  - McCandless,Shawn E
AU  - Curtis,Christine A
TI  - Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies
SN  - 1552-4833
PY  - 2011///0315
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child, Preschool
KW  - Chromosome Banding
KW  - Chromosome Breakage
KW  - Chromosome Deletion
KW  - Chromosomes, Artificial, Bacterial
KW  - Chromosomes, Human, Pair 19
KW  - Comparative Genomic Hybridization
KW  - DNA
KW  - Ectodermal Dysplasia
KW  - Female
KW  - Heart Defects, Congenital
KW  - Humans
KW  - Intellectual Disability
KW  - Muscle Hypotonia
KW  - Oligonucleotide Array Sequence Analysis
KW  - Phenotype
KW  - Physical Chromosome Mapping
KW  - Polymorphism, Single Nucleotide
KW  - Severity of Illness Index
N1  - Publication Type: Case Reports; Comparative Study; Journal Article; Review
UR  - https://doi.org/10.1002/ajmg.a.33738
ER  -