Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.

Buckley, R H

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants. [electronic resource] - The Journal of pediatrics Mar 1997 - 378-87 p. digital

Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.

0022-3476

10.1016/s0022-3476(97)70199-9 doi


Adenosine Deaminase--deficiency
Female
Genes, Recessive
Genetic Linkage
Genotype
Humans
Immunoglobulins--blood
Immunophenotyping
Infant
Infant, Newborn
Janus Kinase 3
Male
Phenotype
Protein-Tyrosine Kinases--deficiency
Severe Combined Immunodeficiency--genetics
X Chromosome