TY  - GEN
AU  - Pinz,Hailey
AU  - Pyle,Louise C
AU  - Li,Dong
AU  - Izumi,Kosuke
AU  - Skraban,Cara
AU  - Tarpinian,Jennifer
AU  - Braddock,Stephen R
AU  - Telegrafi,Aida
AU  - Monaghan,Kristin G
AU  - Zackai,Elaine
AU  - Bhoj,Elizabeth J
TI  - De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies
SN  - 1552-4833
PY  - 2019///0228
KW  - Alleles
KW  - Child, Preschool
KW  - Gene Frequency
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Genetic Variation
KW  - Genotype
KW  - Heart Defects, Congenital
KW  - diagnosis
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - genetics
KW  - Mutation
KW  - Phenotype
KW  - Syndrome
KW  - Transcription Factors
KW  - Urogenital Abnormalities
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1002/ajmg.a.38620
ER  -