« Previous
Next »
The Journal of Allergy and Clinical Immunology
Volume 108, Issue 2
, Pages 310-312
, August 2001
T-cell apoptosis in ICF syndrome
References
- . Multibranched chromosomes 1, 9 and 16 in a patient with combined IgA and IgE deficiency. Hum Genet. 1979;51:127–137
- ICF syndrome: a new case and review of the literature. Hum Genet. 1994;94:240–246
- Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome: report of two new patients and review of the literature. Eur J Pediatr. 1995;154:840–846
- . ICF syndrome with variable expression in sibs. J Med Genet. 1993;30:429–432
- The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Proc Natl Acad Sci U S A. 1999;96:14412–14417
- Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature. 1999;402:187–191
- Genetic variation in ICF syndrome: evidence for genetic heterogeneity. Hum Mutat. 2000;16:509–517
PII: S0091-6749(01)70086-3
doi: 10.1067/mai.2001.116863
© 2001 Mosby, Inc. All rights reserved.
« Previous
Next »
The Journal of Allergy and Clinical Immunology
Volume 108, Issue 2
, Pages 310-312
, August 2001
