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Mandibular left first molar prosthesis

Known as: 19p 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Identification of der(1;19)(q10;p10) in Five Oligodendrogliomas Suggests Mechanism of Concurrent 1p and 19q Loss
Deletions of portions of chromosomes 1p and 19q are closely associated with the oligodendroglioma histologic phenotype. In most… 
Highly Cited
2004
Highly Cited
2004
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
BackgroundAutism is a neurobehavioral spectrum of phenotypes characterized by deficits in the development of language and social… 
Highly Cited
2003
Highly Cited
2003
A whole-genome scan for obstructive sleep apnea and obesity.
Obstructive sleep apnea (OSA) is a common, chronic, complex disease associated with serious cardiovascular and neuropsychological… 
Highly Cited
2001
Highly Cited
2001
Molecular cytogenetic analysis of non-small cell lung carcinoma by spectral karyotyping and comparative genomic hybridization.
Highly Cited
2001
Highly Cited
2001
Chromosomal alterations in lung adenocarcinoma from smokers and nonsmokers.
The etiology of lung tumors arising in nonsmokers remains unclear. Although mutations in the K-ras and p53 genes have been… 
Highly Cited
2000
Highly Cited
2000
Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data.
Breast cancer cell lines provide a useful starting point for the discovery and functional analysis of genes involved in breast… 
Highly Cited
1998
Highly Cited
1998
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.
Febrile convulsions are a common form of childhood seizure. It is estimated that between 2 and 5% of children will have a febrile… 
Highly Cited
1996
Highly Cited
1996
Distinct patterns of chromosomal alterations in high- and low-grade head and neck squamous cell carcinomas.
Comparative genomic hybridization was performed on 30 primary head and neck squamous cell carcinomas. Fractional or entire DNA… 
Highly Cited
1995
Highly Cited
1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.
Hereditary multiple exostosis (EXT) is an autosomal dominant disorder characterized by bony exostoses at the ends of the long… 
Highly Cited
1995
Highly Cited
1995
Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomas.
To gain a better understanding of genetic changes in squamous cell carcinomas of the head and neck we used comparative genomic… 
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