TY  - GEN
AU  - Aref-Eshghi,Erfan
AU  - Bend,Eric G
AU  - Colaiacovo,Samantha
AU  - Caudle,Michelle
AU  - Chakrabarti,Rana
AU  - Napier,Melanie
AU  - Brick,Lauren
AU  - Brady,Lauren
AU  - Carere,Deanna Alexis
AU  - Levy,Michael A
AU  - Kerkhof,Jennifer
AU  - Stuart,Alan
AU  - Saleh,Maha
AU  - Beaudet,Arthur L
AU  - Li,Chumei
AU  - Kozenko,Maryia
AU  - Karp,Natalya
AU  - Prasad,Chitra
AU  - Siu,Victoria Mok
AU  - Tarnopolsky,Mark A
AU  - Ainsworth,Peter J
AU  - Lin,Hanxin
AU  - Rodenhiser,David I
AU  - Krantz,Ian D
AU  - Deardorff,Matthew A
AU  - Schwartz,Charles E
AU  - Sadikovic,Bekim
TI  - Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions
SN  - 1537-6605
PY  - 2020///0203
KW  - Cohort Studies
KW  - Computer Simulation
KW  - Congenital Abnormalities
KW  - diagnosis
KW  - DNA Copy Number Variations
KW  - DNA Methylation
KW  - Epigenomics
KW  - Gene Dosage
KW  - Genetic Diseases, Inborn
KW  - Genetic Variation
KW  - Genome-Wide Association Study
KW  - Genomic Imprinting
KW  - Humans
KW  - Phenotype
KW  - Sequence Analysis, DNA
KW  - Syndrome
KW  - Trinucleotide Repeat Expansion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2019.03.008
ER  -