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Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance.

Publication ,  Journal Article
Buckley, RH; Gard, S; Haynes, BF; Sindel, LJ; Davis, K; Sampson, HA; Ruff, ME; Koren, HS
Published in: Birth Defects Orig Artic Ser
1983

Duke Scholars

Published In

Birth Defects Orig Artic Ser

ISSN

0547-6844

Publication Date

1983

Volume

19

Issue

3

Start / End Page

101 / 104

Location

United States

Related Subject Headings

  • Time Factors
  • Phenotype
  • Leukocyte Count
  • Killer Cells, Natural
  • Infant, Newborn
  • Infant
  • Immunologic Deficiency Syndromes
  • Humans
  • Flow Cytometry
  • Female
 

Citation

APA
Chicago
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MLA
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Buckley, R. H., Gard, S., Haynes, B. F., Sindel, L. J., Davis, K., Sampson, H. A., … Koren, H. S. (1983). Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance. Birth Defects Orig Artic Ser, 19(3), 101–104.
Buckley, R. H., S. Gard, B. F. Haynes, L. J. Sindel, K. Davis, H. A. Sampson, M. E. Ruff, and H. S. Koren. “Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance.Birth Defects Orig Artic Ser 19, no. 3 (1983): 101–4.
Buckley RH, Gard S, Haynes BF, Sindel LJ, Davis K, Sampson HA, et al. Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance. Birth Defects Orig Artic Ser. 1983;19(3):101–4.
Buckley, R. H., et al. “Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance.Birth Defects Orig Artic Ser, vol. 19, no. 3, 1983, pp. 101–04.
Buckley RH, Gard S, Haynes BF, Sindel LJ, Davis K, Sampson HA, Ruff ME, Koren HS. Severe combined immunodeficiency (SCID) with natural killer (NK) cell predominance. Birth Defects Orig Artic Ser. 1983;19(3):101–104.

Published In

Birth Defects Orig Artic Ser

ISSN

0547-6844

Publication Date

1983

Volume

19

Issue

3

Start / End Page

101 / 104

Location

United States

Related Subject Headings

  • Time Factors
  • Phenotype
  • Leukocyte Count
  • Killer Cells, Natural
  • Infant, Newborn
  • Infant
  • Immunologic Deficiency Syndromes
  • Humans
  • Flow Cytometry
  • Female