subject area of
- A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression Academic Article
- A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression Academic Article
- Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: Evidence for additional functions of EYS Academic Article
- Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis Academic Article
- Defining a 0.5-Mb Region of Genomic Gain on Chromosome 6p22 in Bladder Cancer by Quantitative-Multiplex Polymerase Chain Reaction Academic Article
- Epigenetic Profiling in Severe Sepsis: A Pilot Study of DNA Methylation Profiles in Critical Illness* Academic Article
- Epigenetic Profiling in Severe Sepsis: A Pilot Study of DNA Methylation Profiles in Critical Illness. Academic Article
- Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 Academic Article
- Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Academic Article
- HLA-DRnegative, CD34negative Hypergranular Acute Myeloid Leukemia With Trisomy 6 and del(5)(q22q33) Academic Article
- Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker Academic Article
- Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients Academic Article
- Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance Academic Article
- The genetics of hemoglobin A2regulation in sickle cell anemia Academic Article