Genetics of human X-linked immunodeficiency diseases
- PMID: 1863997
- PMCID: PMC1535742
- DOI: 10.1111/j.1365-2249.1991.tb05702.x
Genetics of human X-linked immunodeficiency diseases
Similar articles
-
Molecular genetic analysis of X-linked immunodeficiencies.Year Immunol. 1993;7:162-7. Year Immunol. 1993. PMID: 8372504 Review. No abstract available.
-
[Immunologic diseases with sex-linked heredity; current possibilities for prevention].Ned Tijdschr Geneeskd. 1987 Oct 17;131(42):1849-53. Ned Tijdschr Geneeskd. 1987. PMID: 3670496 Dutch. No abstract available.
-
Experiments of nature: primary immune defects deciphered and defeated.Immunol Rev. 2000 Dec;178:5-7. doi: 10.1034/j.1600-065x.2000.17816.x. Immunol Rev. 2000. PMID: 11213807 Review. No abstract available.
-
Immunodeficiency syndromes. X-linked agammaglobulinemia, common variable immunodeficiency, Chédiak-Higashi syndrome, Wiskott-Aldrich syndrome, and X-linked lymphoproliferative disorder.Dermatol Clin. 1995 Jan;13(1):65-71. Dermatol Clin. 1995. PMID: 7712652 Review.
-
Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.Immunodeficiency. 1993;4(1-4):213-5. Immunodeficiency. 1993. PMID: 8167703
Cited by
-
Mapping of the X linked form of hyper IgM syndrome (HIGM1).J Med Genet. 1993 Mar;30(3):202-5. doi: 10.1136/jmg.30.3.202. J Med Genet. 1993. PMID: 8097258 Free PMC article.
-
Knockout of Rlim Results in a Sex Ratio Shift toward Males but Superovulation Cannot Compensate for the Reduced Litter Size.Animals (Basel). 2023 Mar 17;13(6):1079. doi: 10.3390/ani13061079. Animals (Basel). 2023. PMID: 36978620 Free PMC article.
-
Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.J Clin Invest. 1993 Apr;91(4):1616-29. doi: 10.1172/JCI116369. J Clin Invest. 1993. PMID: 8473505 Free PMC article.
-
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.Hum Genet. 1991 Nov;88(1):105-11. doi: 10.1007/BF00204939. Hum Genet. 1991. PMID: 1959916
-
X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.Eur J Pediatr. 1993 Nov;152(11):900-4. doi: 10.1007/BF01957526. Eur J Pediatr. 1993. PMID: 8276019
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources