4q35.1

Chromosome 4q deletion syndrome (4q‐ syndrome) is a rare condition, with an estimated incidence of 1 in 100,000. Although… Expand

Chien W‐H, Gau SS‐F, Wu Y‐Y, Huang Y‐S, Fang J‐S, Chen Y‐J, Soong W‐T, Chiu Y‐N, Chen C‐H. Identification and molecular… Expand

BackgroundLoss of heterozygosity (LOH) in the ING family members has been shown in head and neck squamous cell carcinoma (HNSCC… Expand

Chromosomal instability, manifesting as copy number alterations (CNAs), is characteristic of pancreatic adenocarcinoma. We used… Expand

Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy characterized by multiple glistening… Expand

Myelodysplasia/acute myeloid leukemia (MDS/AML) is characterized by a t(3;5)(q25.1;q34) chromosomal translocation that forms a… Expand

Microarray analyses combined with laser-capture microdissection have been applied for risk assessments of gastric cancer as well… Expand

Low copy repeats (LCRs) located in 22q11.2, especially LCR-B, are susceptible to rearrangements associated with several… Expand

The pineal hormone melatonin elicits potent circadian and reproductive effects in mammals. We report the chromosomal location of… Expand

Interferon regulatory factor 1 (IRF-1) and IRF-2 are structurally similar DNA-binding factors which were originally identified as… Expand