Skip to main content

. 1995 Feb;95(2):443–444. doi: 10.1172/JCI117682

Genetic mosaicism: what Gregor Mendel didn't know.

PMCID: PMC295484 PMID: 7860724

443

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Hall J. G. Review and hypotheses: somatic mosaicism: observations related to clinical genetics. Am J Hum Genet. 1988 Oct;43(4):355–363. [PMC free article] [PubMed] [Google Scholar]
Hirschhorn R., Yang D. R., Israni A., Huie M. L., Ownby D. R. Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery. Am J Hum Genet. 1994 Jul;55(1):59–68. [PMC free article] [PubMed] [Google Scholar]
Huie M. L., Chen A. S., Brooks S. S., Grix A., Hirschhorn R. A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII). Hum Mol Genet. 1994 Jul;3(7):1081–1087. doi: 10.1093/hmg/3.7.1081. [DOI] [PubMed] [Google Scholar]
Kvittingen E. A., Rootwelt H., Berger R., Brandtzaeg P. Self-induced correction of the genetic defect in tyrosinemia type I. J Clin Invest. 1994 Oct;94(4):1657–1661. doi: 10.1172/JCI117509. [DOI] [PMC free article] [PubMed] [Google Scholar]
Puck J. M., Pepper A. E., Bédard P. M., Laframboise R. Female germ line mosaicism as the origin of a unique IL-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency. J Clin Invest. 1995 Feb;95(2):895–899. doi: 10.1172/JCI117740. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES