Related Experiment Videos
New approaches to evaluating the genetic effects of the atomic bombs
American Journal of Human Genetics
|December 1, 1995
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Analysis of human peripheral blood T cells and single-cell-derived T cell clones uncovers extensive clonal CpG island methylation heterogeneity throughout the genome.
Proceedings of the National Academy of Sciences of the United States of America·1999
JC virus DNA is present in the mucosa of the human colon and in colorectal cancers.
Proceedings of the National Academy of Sciences of the United States of America·1999
The JC and BK human polyoma viruses appear to be recent introductions to some South American Indian tribes: there is no serological evidence of cross-reactivity with the simian polyoma virus SV40.
Proceedings of the National Academy of Sciences of the United States of America·1998
Syndrome X: is it for real?
Genetic epidemiology·1998
Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.
American journal of human genetics·2026
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.
American journal of human genetics·2026
RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium.
American journal of human genetics·2026
Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes.
American journal of human genetics·2026
Shared genetic basis and structure of syndromic and normal facial variation.
American journal of human genetics·2026
The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.
American journal of human genetics·2026
Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.
Frontiers in cell and developmental biology·2026
Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.
Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo·2026
A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.
Medicina (Kaunas, Lithuania)·2026