Skip to search formSkip to main contentSkip to account menu

19q13.2

A chromosome band present on 19q
National Institutes of Health

Related topics

Related topics

23 relations
19qAPOE wt AlleleAPOE*4 AlleleB9D2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Gene involvement in cleft lip and palate (CLP) patients
It is supposed that the most frequent birth defect worldwide is clefts of the lip and/or palate (CL+-P). The frequency is non… 
2006
2006
Proximal 19q Trisomy: A New Syndrome of Morbid Obesity and Mental Retardation
Aims: To report on the clinical and metabolic characteristic and the unique chromosomal defect of a mentally retarded and… 
2005
2005
Characterization of drug-resistant neuroblastoma cell lines by comparative genomic hybridization.
Three parental neuroblastoma cell lines and nine derived lines resistant to Vincristin, Doxorubicin and Cisplatin, respectively… 
2004
2004
Linkage analysis between BCL3 and nearby genes on 19q13.2 and non-syndromic cleft lip with or without cleft palate in multigenerational Japanese families.
OBJECTIVE To investigate the linkage between candidate genes on chromosome 19 and cleft lip with or without cleft palate in… 
2003
2003
Twelve Single Nucleotide Polymorphisms on Chromosome 19q13.2-13.3: Linkage Disequilibria and Associations with Basal Cell Carcinoma in Danish Psoriatic Patients
The genetic susceptibility to basal cell carcinoma (BCC) among Danish psoriatic patients was investigated in association studies… 
1999
1999
A microdeletion syndrome due to a 3‐Mb deletion on 19q13.2 – Diamond–Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation
We report on a boy with congenital pure red blood cell aplasia [Diamond–Blackfan anemia (DBA)] and severe congenital hypotonia… 
Highly Cited
1994
Highly Cited
1994
Molecular cloning of a human transmembrane-type protein tyrosine phosphatase and its expression in gastrointestinal cancers.
1991
1991
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.
1990
1990
Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region.
Hybridization studies using a panel of somatic cell hybrids with subchromosomal segments of 19q have localized the genes encoding… 
Highly Cited
1989
Highly Cited
1989
Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.
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)