TY  - GEN
AU  - Elliott,David A
AU  - Kirk,Edwin P
AU  - Yeoh,Thomas
AU  - Chandar,Suchitra
AU  - McKenzie,Fiona
AU  - Taylor,Peter
AU  - Grossfeld,Paul
AU  - Fatkin,Diane
AU  - Jones,Owen
AU  - Hayes,Peter
AU  - Feneley,Michael
AU  - Harvey,Richard P
TI  - Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome
SN  - 0735-1097
PY  - 2003///0718
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Australia
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Family Health
KW  - Female
KW  - Genes, Homeobox
KW  - genetics
KW  - Genetic Markers
KW  - Heart Block
KW  - Heart Conduction System
KW  - pathology
KW  - Heart Defects, Congenital
KW  - Heart Septal Defects, Atrial
KW  - Homeobox Protein Nkx-2.5
KW  - Homeodomain Proteins
KW  - Humans
KW  - Hypoplastic Left Heart Syndrome
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Middle Aged
KW  - Point Mutation
KW  - Polymorphism, Genetic
KW  - Retrospective Studies
KW  - Statistics as Topic
KW  - Transcription Factors
KW  - United States
KW  - Xenopus Proteins
N1  - Publication Type: Comparative Study; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1016/s0735-1097(03)00420-0
ER  -