TY  - GEN
AU  - Lehman,A M
AU  - du Souich,C
AU  - Chai,D
AU  - Eydoux,P
AU  - Huang,J L
AU  - Fok,A K
AU  - Avila,L
AU  - Swingland,J
AU  - Delaney,A D
AU  - McGillivray,B
AU  - Goldowitz,D
AU  - Argiropoulos,B
AU  - Kobor,M S
AU  - Boerkoel,C F
TI  - 19p13.2 microduplication causes a Sotos syndrome-like phenotype and alters gene expression
SN  - 1399-0004
PY  - 2012///0405
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Alu Elements
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Duplication
KW  - Chromosomes, Human, Pair 19
KW  - genetics
KW  - Craniofacial Abnormalities
KW  - DNA (Cytosine-5-)-Methyltransferase 1
KW  - DNA (Cytosine-5-)-Methyltransferases
KW  - DNA Methylation
KW  - DNA Mutational Analysis
KW  - Female
KW  - Gene Expression Regulation
KW  - Genome, Human
KW  - Humans
KW  - Infant
KW  - Learning Disabilities
KW  - Leukocytes, Mononuclear
KW  - cytology
KW  - Male
KW  - Middle Aged
KW  - Oligonucleotide Array Sequence Analysis
KW  - Pedigree
KW  - Phenotype
KW  - Sotos Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2010.01615.x
ER  -