Skip to search formSkip to main contentSkip to account menu

14q24

A chromosome band present on 14q
National Institutes of Health

Related topics

Related topics

5 relations
ChromosomesLTBP2 wt AlleleMTHFD1 wt AlleleTGFB3 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Toward Primary Congenital Glaucoma GLC 3 B Gene Identification : The Case of Kazrin Gene
Primary Congenital Glaucoma (PCG) is an ocular disease that occurs before the age of 3 years, and results from malformation of… 
2008
2008
The breakpoints of spontaneous chromosome aberrations in lymphocytes from patients with non-Hodgkin's lymphoma are nonrandomly distributed.
The distribution of breakpoints in spontaneous chromosome aberrations (chromatid and chromosome gaps, breaks, and exchanges) was… 
2008
2008
Breakprone chromosome bands in lymphocytes from sarcoma patients do not coincide with bands involved in primary sarcoma-associated chromosome rearrangements.
The localization of breakpoints in spontaneous chromosome aberrations, i.e., chromatid and chromosome gaps, breaks, and exchanges… 
2003
2003
Genetic Modifiers of the Age at Diagnosis of Diabetes ( MODY 3 ) in Carriers of Hepatocyte Nuclear Factor-1 Mutations Map to Chromosomes 5 p 15 , 9 q 22 , and 14 q 24
Mutations in hepatocyte nuclear factor (HNF)-1 (MODY3) account for the largest proportion of maturity-onset diabetes of the young… 
Review
2003
Review
2003
Epigenetics: Breaking the silence
86 | FEBRUARY 2003 | VOLUME 3 www.nature.com/reviews/cancer Epigenetic modifications, such as DNA hypermethylation and histone… 
2002
2002
Lipomatous Hamartoma a Rare Reason of Endobronchial Occlusion
Most tumors of the tracheobronchial tree aremalignant in nature. Benign endobronchialtumors are rare and there is… 
2001
2001
Molecular Cytogenetic Characterization of Head and Neck Squamous Cell Carcinoma and Refinement of 3 q Amplification 1
We applied a combination of molecular cytogenetic methods, including comparative genomic hybridization (CGH), spectral… 
1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
  • 1998
  • Corpus ID: 262018442
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without… 
1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without… 
1983
1983
Tandem duplication of chromosome 14 (q24 leads to q32) in male newborn with congenital malformations.
A tandem duplication of 14q24 leads to q32, estimated by G- and R-banding, was found in a male newborn with growth retardation… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)