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Mandibular left first molar prosthesis
Known as:
19p
National Institutes of Health
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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
C. Griffin
,
P. Burger
,
+4 authors
K. Murphy
Journal of neuropathology and experimental…
2006
Corpus ID: 44614820
Deletions of portions of chromosomes 1p and 19q are closely associated with the oligodendroglioma histologic phenotype. In most…
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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
J. McCauley
,
Chun Xing Li
,
+6 authors
J. Sutcliffe
BMC Medical Genetics
2004
Corpus ID: 1228384
BackgroundAutism is a neurobehavioral spectrum of phenotypes characterized by deficits in the development of language and social…
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Highly Cited
2003
Highly Cited
2003
A whole-genome scan for obstructive sleep apnea and obesity.
L. Palmer
,
S. Buxbaum
,
+4 authors
S. Redline
American journal of human genetics
2003
Corpus ID: 22836319
Obstructive sleep apnea (OSA) is a common, chronic, complex disease associated with serious cardiovascular and neuropsychological…
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Highly Cited
2001
Highly Cited
2001
Molecular cytogenetic analysis of non-small cell lung carcinoma by spectral karyotyping and comparative genomic hybridization.
C. Luk
,
M. Tsao
,
J. Bayani
,
F. Shepherd
,
J. Squire
Cancer genetics and cytogenetics
2001
Corpus ID: 43166073
Highly Cited
2001
Highly Cited
2001
Chromosomal alterations in lung adenocarcinoma from smokers and nonsmokers.
M. Sanchez-Cespedes
,
S. Ahrendt
,
+7 authors
D. Sidransky
Cancer research
2001
Corpus ID: 7938765
The etiology of lung tumors arising in nonsmokers remains unclear. Although mutations in the K-ras and p53 genes have been…
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Highly Cited
2000
Highly Cited
2000
Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data.
F. Forozan
,
E. Mahlamäki
,
+7 authors
O. Kallioniemi
Cancer research
2000
Corpus ID: 16313142
Breast cancer cell lines provide a useful starting point for the discovery and functional analysis of genes involved in breast…
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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.
E. Johnson
,
J. Dubovský
,
+8 authors
J. Weber
Human molecular genetics
1998
Corpus ID: 17564655
Febrile convulsions are a common form of childhood seizure. It is estimated that between 2 and 5% of children will have a febrile…
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Highly Cited
1996
Highly Cited
1996
Distinct patterns of chromosomal alterations in high- and low-grade head and neck squamous cell carcinomas.
U. Bockmühl
,
A. Schwendel
,
M. Dietel
,
I. Petersen
Cancer research
1996
Corpus ID: 16451390
Comparative genomic hybridization was performed on 30 primary head and neck squamous cell carcinomas. Fractional or entire DNA…
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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.
J. Hecht
,
D. Hogue
,
L. Strong
,
M. Hansen
,
S. Blanton
,
M. Wagner
American journal of human genetics
1995
Corpus ID: 24205612
Hereditary multiple exostosis (EXT) is an autosomal dominant disorder characterized by bony exostoses at the ends of the long…
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Highly Cited
1995
Highly Cited
1995
Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomas.
M. Speicher
,
C. Howe
,
P. Crotty
,
S. du Manoir
,
J. Costa
,
D. Ward
Cancer research
1995
Corpus ID: 23416431
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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