Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Z E, Karanjawala"'
Autor:
K. A. Savin, Donald R. Deardorff, D. C. Hager, Z. E. Karanjawala, J. E. Ii Sheppeck, N. Aydin, C. J. Justman
Publikováno v:
ChemInform. 27
Autor:
Z E, Karanjawala, H, Kääriäinen, S, Ghosh, J, Tannenbaum, C, Martin, D, Ally, J, Tuomilehto, T, Valle, F S, Collins
Publikováno v:
American journal of medical genetics. 93(3)
Uniparental disomy (UPD) is a condition in which diploid individuals possess a chromosome pair from a single parent. In some instances, UPD causes an abnormal phenotype due to imprinting effects, reduction to homozygosity at recessive disease loci, o
Autor:
S, Ghosh, R M, Watanabe, T T, Valle, E R, Hauser, V L, Magnuson, C D, Langefeld, D S, Ally, K L, Mohlke, K, Silander, K, Kohtamäki, P, Chines, J, Balow, G, Birznieks, J, Chang, W, Eldridge, M R, Erdos, Z E, Karanjawala, J I, Knapp, K, Kudelko, C, Martin, A, Morales-Mena, A, Musick, T, Musick, C, Pfahl, R, Porter, J B, Rayman
Publikováno v:
American journal of human genetics. 67(5)
We performed a genome scan at an average resolution of 8 cM in 719 Finnish sib pairs with type 2 diabetes. Our strongest results are for chromosome 20, where we observe a weighted maximum LOD score (MLS) of 2.15 at map position 69.5 cM from pter and