Skip to search formSkip to main contentSkip to account menu

16q24.1

Part of the chromosome bands present on the long (q) arm of chromosome 16.
National Institutes of Health

Related topics

Related topics

5 relations
16qATP2C2 wt AlleleChromosomesIRF8 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare cause of pulmonary hypertension in newborns… 
2016
2016
Leaky transporters and sphincters in Barrett's oesophagus?
2013
2013
Identification of three novel frameshift mutations of the MVK gene in four Chinese families with disseminated superficial actinic porokeratosis
MADAM, Porokeratosis is a group of hereditary disorders of epidermal keratinization, characterized by keratotic lesions with an… 
2013
2013
Inversion upstream of FOXF1 in a case of lethal alveolar capillary dysplasia with misalignment of pulmonary veins
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a congenital malformation that leads to severe… 
2013
2013
Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement
Clinical and Cytogenetic Characterization of a Boy With a De Novo Pure Partial Trisomy 16q24.1q24.3 and Complex Chromosome… 
2012
2012
Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes
We report the prenatal diagnosis of cystic hygroma that was subsequently identified to have haploinsufficiency of the FOXF1 and… 
2010
2010
Summary of "Genomic and genetic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations".
The gastrointestinal (GI) tract develops from the embryonic endoderm (which gives rise to the epithelium) and the visceral… 
2001
2001
Abnormal Expression of 17-Hydroxysteroid Dehydrogenases in Breast Cancer Predicts Late Recurrence 1
The 17 -hydroxysteroid dehydrogenase (17 -HSD) enzymes are involved in the interconversion of biologically active and inactive… 
2000
2000
Identification of a 1‐Mb common region at 16q24.1–24.2 deleted in hepatocellular carcinoma
To identify the location of one or more putative tumor suppressor genes that may be involved in hepatocellular carcinoma (HCC… 
1994
1994
Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse.
We have mapped the PLCG2 gene, which encodes the enzyme phosphatidyl inositol-specific phospholipase C-gamma 2. This is one of… 
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)