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Familial Cancer|May 24, 2014
Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samplesKristóf Arvai, Péter Horváth, Bernadett Balla, et al.
Familial Cancer|May 20, 2014
Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palateKamil K Hozyasz, Adrianna Mostowska, Piotr Wójcicki, et al.
Familial Cancer|October 23, 2012
Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrierShaheen Alanee, Sohela Shah, Rajmohan Murali, et al.
Familial Cancer|January 24, 2015
The effect of oral 3,3'-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriersDina Nikitina, Marcia Llacuachaqui, Daniel Sepkovic, et al.
Familial Cancer|August 7, 2012
Non-synonymous polymorphism (Gln261Arg) of 12-lipoxygenase in colorectal and thyroid cancersVidudala V T S Prasad, Kolli Padma
Familial Cancer|August 7, 2012
Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutationChristina Therkildsen, Anna Isinger-Ekstrand, Steen Ladelund, et al.
Familial Cancer|July 26, 2012
Portuguese c.156_157insAlu BRCA2 founder mutation: gastrointestinal and tongue neoplasias may be part of the phenotypeMiguel A M Moreira, Irina G Bobrovnitchaia, Maria Angélica F D Lima, et al.
Familial Cancer|July 26, 2012
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminomaStephanie Smetsers, Joanne Muter, Claire Bristow, et al.
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