4q35.1

Obesity Syndrome, MOMES Caused by Deletion–Duplication (4q35.1 del and 5p14.3 dup) Mieke M. van Haelst, Rubin Wang, Piranit N… (More)

Loss of heterozygosity (LOH) in the ING family members has been shown in head and neck squamous cell carcinoma (HNSCC) except for… (More)

BACKGROUND & AIMS Neonatal intestinal obstruction (meconium ileus [MI]) occurs in 15% of patients with cystic fibrosis (CF). Our… (More)

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

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

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

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

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

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

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