Identification of germline genomic copy number variation in familial pancreatic cancer.
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Rare Germline Copy Number Variations and Disease Susceptibility in Familial MelanomaGenetic and molecular alterations in pancreatic cancer: implications for personalized medicine.Familial pancreatic cancer: genetic advances.The association of copy number variation and percent mammographic densityProlonged survival and delayed progression of pancreatic intraepithelial neoplasia in LSL-KrasG12D/+;Pdx-1-Cre mice by vitamin E δ-tocotrienol.Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk.Familial pancreatic cancer: challenging diagnostic approach and therapeutic management.Genome-wide association studies and epigenome-wide association studies go together in cancer control.Chronic pancreatitis and lipomatosis are associated with defective function of ciliary genes in pancreatic ductal cells.Application of Machine Learning to Development of Copy Number Variation-based Prediction of Cancer RiskGermline copy number variations are associated with breast cancer risk and prognosis.Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.
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Identification of germline genomic copy number variation in familial pancreatic cancer.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 05 June 2012
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Identification of germline genomic copy number variation in familial pancreatic cancer.
@en
Identification of germline genomic copy number variation in familial pancreatic cancer.
@nl
type
label
Identification of germline genomic copy number variation in familial pancreatic cancer.
@en
Identification of germline genomic copy number variation in familial pancreatic cancer.
@nl
prefLabel
Identification of germline genomic copy number variation in familial pancreatic cancer.
@en
Identification of germline genomic copy number variation in familial pancreatic cancer.
@nl
P2093
P2860
P1433
P1476
Identification of germline genomic copy number variation in familial pancreatic cancer.
@en
P2093
Aaron Gropper
Alison P Klein
Anath C Lionel
Ann G Schwartz
Ayelet Borgida
Christian R Marshall
George Zogopoulos
Gloria M Petersen
Kari G Rabe
Melissa Bondy
P2860
P2888
P304
P356
10.1007/S00439-012-1183-1
P577
2012-06-05T00:00:00Z