HD21 HUMAN VARIATION PANEL

Description: HUMAN VARIATION PANEL - ITALIAN

Aliquot Size: 10 µg each

Sex: Males: 4 Females: 6

Brief Description: Some samples in the Human Variation Collection have been assigned a second catalogue number to indicate inclusion in the Human Variation Collection in addition to their original catalogue number. A complete list of the alternative sample numbers can be downloaded as an Excel file.
Visscher, H., Ross, C.J.D., Dube, M-P., Brown, A.M.K., Phillips, M.S., Carleton, B.C., and Hayden, M.R., Application of principal component analysis to pharmacogenomic studies in Canada The Pharmacogenomics Journal9:362-372 2009
PubMed ID: 19652663
 
Bauchet, M., McEvoy, B., Pearson, L.N., Quillen, E.E., Sarkisian, T., Hovhannesyan, K., Deka, R., Bradley, D.G. and Shriver, M.D., Measuring European population stratification with microarray genotype data Am J Hum Genet80:948-956 2007
PubMed ID: 17436249
 
Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, Chokkalingam AP, Alexander HC, Ardlie KG, Huang Q, Smith AM, Spoerke JM, Conn MT, Chang M, Chang SY, Saiki RK, Catanese JJ, Leong DU, Garcia VE, McAllister LB, Jeffery DA, Lee AT, Batliwalla F, Remmers E, Criswell LA, Seldin MF, Kastner DL, Amos CI, Sninsky JJ, Gregersen PK, A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis. Am J Hum GenetEpub ahead of print:948-956 2004
PubMed ID: 15208781
 
Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM, Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin. Am J Hum Genet71(3):618-24 2002
PubMed ID: 12089654

Catalog IDSexAge at Sampling
NA17321Female55 YR
NA17322Female54 YR
NA17323Female40 YR
NA17330Female35 YR
NA17327Female25 YR
NA17328Female25 YR
NA17329Male8 YR
NA17324Male34 YR
NA17325Male33 YR
NA17326Male