TY  - GEN
AU  - Lammer,E J
AU  - Scholes,T
AU  - Abrams,L
TI  - Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?
SN  - 0962-8827
PY  - 2001///0315
KW  - Adolescent
KW  - Child
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Genes, Recessive
KW  - Humans
KW  - Hydrocephalus
KW  - diagnosis
KW  - Infant
KW  - Infant, Newborn
KW  - Language Development Disorders
KW  - Male
KW  - Nuclear Family
KW  - Pedigree
KW  - Syndrome
KW  - Tetralogy of Fallot
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1097/00019605-200101000-00002
ER  -