TY  - GEN
AU  - Hjelle,B
AU  - Charache,S
AU  - Phillips,J A
TI  - Hemoglobin H disease and multiple congenital anomalies in a child of northern European origin
SN  - 0361-8609
PY  - 1983///0311
KW  - Abnormalities, Multiple
KW  - blood
KW  - Child
KW  - DNA
KW  - genetics
KW  - Genotype
KW  - Hemoglobin H
KW  - analysis
KW  - Humans
KW  - Male
KW  - Nucleic Acid Hybridization
KW  - Pedigree
KW  - Thalassemia
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ajh.2830130407
ER  -