X-Linked Immunodeficiencies

Author:

Puck Jennifer M.

Publisher

Springer US

Reference113 articles.

1. Anderson, W F, 1990, September 14, 1990: The beginningGene Ther. 1:371–372.

2. Arveiler, B., De Saint Basile, G., Fischer, A., Griscelli, C., and Mandel, I-L., 1990, Germ-line mosaicism simulates genetic heterogeneity in Wiskott—Aldrich syndromeAm. J. Hum. Genet. 46:906–911.

3. Baehner, R. L., 1990, Chronic granulomatous disease of childhood: Clinical, pathological, biochemical, molecular, and genetic aspects of the diseasePediatr. Pathol. 10:143–154.

4. Blakemore, K., Scioscia, A., Grannum, P., Podell, D., Hobbins, J., and Mahoney, M., 1987, The value of fetal blood sampling in the prenatal diagnosis of severe combined immunodeficiency syndromeAm. J. Hum. Genet. 41(Suppl):A267.

5. Boyd, Y., and Fraser, N. J., 1990, Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27b): Correlation with X-inactivation statusGenomics 7:182–187.

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