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XC01331 CEPH FAMILY KIT

Description: CEPH/UTAH PEDIGREE 1331

Aliquot Size: 10 µg each

Pricing
Commercial/For-profit:
$2,535.00USD
Academic/Non-profit/Government:
$1,271.00USD
Add to Cart
  • Publications
Tremblay DC, Alexander G, Moseley S, Chadwick BP, Expression, tandem repeat copy number variation and stability of four macrosatellite arrays in the human genome BMC genomics11:632 2010
PubMed ID: 21078170
 
Duan S, Bleibel WK, Huang RS, Shukla SJ, Wu X, Badner JA, Dolan ME, Mapping genes that contribute to daunorubicin-induced cytotoxicity Cancer research67:5425-33 2007
PubMed ID: 17545624
 
Audrain-McGovern J, Rodriguez D, Wileyto EP, Schmitz KH, Shields PG, Effect of team sport participation on genetic predisposition to adolescent smoking progression Archives of general psychiatry63:433-41 2006
PubMed ID: 16585473
 
Busiello R, Fimiani G, Miano MG, Aricò M, Santoro A, Ursini MV, Pignata C, A91V perforin variation in healthy subjects and FHLH patients International journal of immunogenetics33:123-5 2006
PubMed ID: 16611257
 
Zubenko GS, Hughes HB, Zubenko WN, Maher BS, Genome survey for loci that influence successful aging: results at 10-cM resolution The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry15:184-93 2006
PubMed ID: 16905685
 
Rennert H, Zeigler-Johnson CM, Addya K, Finley MJ, Walker AH, Spangler E, Leonard DG, Wein A, Malkowicz SB, Rebbeck TR, Association of susceptibility alleles in ELAC2/HPC2, RNASEL/HPC1, and MSR1 with prostate cancer severity in European American and African American men Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology14:949-57 2005
PubMed ID: 15824169
 
Savage SA, Stewart BJ, Eckert A, Kiley M, Liao JS, Chanock SJ, Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint Human mutation26:343-50 2005
PubMed ID: 16110488
 
Dolan ME, Newbold KG, Nagasubramanian R, Wu X, Ratain MJ, Cook EH, Badner JA, Heritability and linkage analysis of sensitivity to cisplatin-induced cytotoxicity Cancer research64:4353-6 2004
PubMed ID: 15205351
 
Zhou L, Vandersteen J, Wang L, Fuller T, Taylor M, Palais B, Wittwer CT, High-resolution DNA melting curve analysis to establish HLA genotypic identity Tissue antigens64:156-64 2004
PubMed ID: 15245370
 
Schork NJ, Gardner JP, Zhang L, Fallin D, Thiel B, Jakubowski H, Aviv A, Genomic association/linkage of sodium lithium countertransport in CEPH pedigrees. Hypertension40(5):619-28 2002
PubMed ID: 12411453
 
Butkiewicz D, Rusin M, Enewold L, Shields PG, Chorazy M, Harris CC, Genetic polymorphisms in DNA repair genes and risk of lung cancer. Carcinogenesis22(4):593-7 2001
PubMed ID: 11285194
 
Seker H, Butkiewicz D, Bowman ED, Rusin M, Hedayati M, Grossman L, Harris CC, Functional significance of XPD polymorphic variants: attenuated apoptosis in human lymphoblastoid cells with the XPD 312 Asp/Asp genotype. Cancer Res61(20):7430-4 2001
PubMed ID: 11606376
 
Wang WW, Spurdle AB, Kolachana P, Bove B, Modan B, Ebbers SM, Suthers G, Tucker MA, Kaufman DJ, Doody MM, Tarone RE, Daly M, Levavi H, Pierce H, Chetrit A, Yechezkel GH, Chenevix-Trench G, Offit K, Godwin AK, Struewing JP, A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers. Cancer Epidemiol Biomarkers Prev10(9):955-60 2001
PubMed ID: 11535547
How to Order
  • Online Ordering
  • Assurance Form
  • Statement of Research Intent Form

Catalog IDSexFamilyRelationship
NA07340Female1331paternal grandmother
NA06990Female1331mother
NA07050Female1331maternal grandmother
NA06988Female1331daughter
NA06999Female1331daughter
NA07005Female1331daughter
NA07023Female1331daughter
NA07059Female1331daughter
NA11818Female1331daughter
NA06983Male1331son
NA06992Male1331son
NA07030Male1331son
NA07033Male1331son
NA11819Male1331son
NA07016Male1331maternal grandfather
NA07057Male1331father

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