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Common variable immunodeficiency (hypogammaglobulinemia) with an autosomal recessive pattern of inheritance

Lokman MN , George R , Sukumaran S , Nasuruddin BA
Med J Malaysia, 1988 Sep;43(3):237-42.
PMID: 3241582

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

MeSH terms
  • Agammaglobulinemia/diagnosis
  • Agammaglobulinemia/genetics*
  • Agammaglobulinemia/immunology
  • Child, Preschool
  • Chromosome Aberrations
  • Female
  • Genes, Recessive*
  • Humans
  • Male
  • Suppressor Factors, Immunologic/physiology
  • Chromosome Disorders
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* MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.