Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia

Lancet. 1968 Mar 9;1(7541):499-503. doi: 10.1016/s0140-6736(68)91467-0.

Authors

J C Jacobs, A de Capoa, E McGilvray, J H Morse, J N Schullinger, W A Blanc, W C Heird, O J Miller, R D Rossen, R A Walzer

PMID: 4170833
DOI: 10.1016/s0140-6736(68)91467-0

No abstract available

MeSH terms

Agammaglobulinemia / complications*
Agammaglobulinemia / genetics
Biological Transport
Blood Group Incompatibility
Chromosome Aberrations*
Chromosome Disorders*
Complement System Proteins*
Fluorescent Antibody Technique
Humans
Infant
Male
Salivary Glands / immunology
Thymus Gland / transplantation
Transplantation, Homologous
gamma-Globulins / analysis

Substances

gamma-Globulins
Complement System Proteins