Hereditary lymphopenic agammaglobulinemia associated with a distinctive form of short-limbed dwarfism and ectodermal dysplasia
- 31 October 1969
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 75 (4), 675-684
- https://doi.org/10.1016/s0022-3476(69)80465-8
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- HAZARDS AND POTENTIAL BENEFITS OF BLOOD-TRANSFUSION IN IMMUNOLOGICAL DEFICIENCYThe Lancet, 1968
- AchondroplasiaClinical Pediatrics, 1968
- LYMPHOPENIC FORMS OF CONGENITAL IMMUNOLOGIC DEFICIENCY DISEASESMedicine, 1968
- Relationship between Thymus and HypophysisNature, 1967
- Hu-1: Major Histocompatibility Locus in ManScience, 1967
- A case of Swiss-type agammaglobulinaemia and achondroplasia.BMJ, 1966
- Ataxia-Telangiectasia and Swiss-Type AgammaglobulinemiaPublished by American Medical Association (AMA) ,1966
- Ataxia-telangiectasia and Swiss-type agammaglobulinemia. Two genetic disorders of the immune mechanism in related Amish sibshipsJAMA, 1966
- Number, size, and distribution of Peyer's patches in the human small intestine: Part I The development of Peyer's patchesGut, 1965
- A Hereditary Factor in Chondrodystrophia Calcificans CongenitaNew England Journal of Medicine, 1954