Elizabeth M. Spiteri, Ph.D.
Affiliations: | 2002 | Yeshiva University, New York, NY, United States |
Area:
GeneticsGoogle:
"Elizabeth Spiteri"Mean distance: 23748
Parents
Sign in to add mentorBernice Morrow | grad student | 2002 | Yeshiva University | |
(Mechanisms of germline translocations in chromosome 22q11.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Church AJ, Akkari Y, Deeb K, et al. (2024) Section E6.7-6.12 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in solid tumors. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101070 |
Babcock M, Pavlicek A, Spiteri E, et al. (2003) Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. Genome Research. 13: 2519-32 |
Allen E, Horvath S, Tong F, et al. (2003) High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes. Proceedings of the National Academy of Sciences of the United States of America. 100: 9940-5 |
Spiteri E, Babcock M, Kashork CD, et al. (2003) Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Human Molecular Genetics. 12: 1823-37 |
Edelmann L, Stankiewicz P, Spiteri E, et al. (2001) Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus Genome Research. 11: 208-217 |
Edelmann L, Spiteri E, Koren K, et al. (2000) AT-rich palindromes mediate the constitutional t(11;22) translocation. American Journal of Human Genetics. 68: 1-13 |
Edelmann L, Spiteri E, McCain N, et al. (1999) A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation. American Journal of Human Genetics. 65: 1608-16 |
Edelmann L, Pandita RK, Spiteri E, et al. (1999) A common molecular basis for rearrangement disorders on chromosome 22q11 Human Molecular Genetics. 8: 1157-1167 |