Zobrazeno 1 - 5
of 5
pro vyhledávání: '"N. M. PEARSON"'
Autor:
Victor Wei Zhang, Ian M. Campbell, Y. Yang, Sherif R. Zaki, Mei W. Baker, Jordan S. Orange, Imelda C. Hanson, Gail J. Demmler-Harrison, Diana K. Bayer, Magalie S. Leduc, Lisa R. Forbes, Filiz O. Seeborg, Christine M. Eng, Olaug K. Rødningen, Ankita Patel, W. J. Bellini, R. A. Gibbs, Caridad Martinez, Donna M. Muzny, Lenora M. Noroski, Chad A. Shaw, Hanne Sørmo Sorte, Asbjørg Stray-Pedersen, James R. Lupski, N. M. Pearson
Publikováno v:
Clinical and Experimental Immunology. 178:459-469
Summary In areas without newborn screening for severe combined immunodeficiency (SCID), disease-defining infections may lead to diagnosis, and in some cases, may not be identified prior to the first year of life. We describe a female infant who prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9855177f0da619a18b287153a2d62e5
https://doi.org/10.1111/cei.12421
https://doi.org/10.1111/cei.12421
Autor:
Tatiana Zerjal, K. Balakrishnan, N M Pearson, I Tsoy, S Gambarov, Nadira Yuldasheva, Ruslan Ruzibakiev, Matthew T. Webster, M Mirrakhimov, Li Jin, Irina Evseeva, A Dostiev, S. Shanmugalakshmi, Ramasamy Pitchappan, Jason Blue-Smith, Walter F. Bodmer, R. S. Wells, Peter A. Underhill, M Read, I Zholoshvili, M Kitaev, O Aknazarov, A Chariev, Bing Su, Pierre Zalloua, B Nikbin, E Jamarjashvili
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 98(18)
The nonrecombining portion of the human Y chromosome has proven to be a valuable tool for the study of population history. The maintenance of extended haplotypes characteristic of particular geographic regions, despite extensive admixture, allows com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::661ea1d9dd8f3d9d15263b58a5cd825f
http://ora.ox.ac.uk/objects/uuid:24973bd2-afb0-451f-83c7-a82381e1ba31
http://ora.ox.ac.uk/objects/uuid:24973bd2-afb0-451f-83c7-a82381e1ba31
Autor:
T. Joyce, N. Solomey, J. H. Hoftiezer, D. S. Ayres, J. L. Thron, W. A. Mann, K. Sivaprasad, I. Ambats, L. E. Price, Edward May, N. M. Pearson, J. W. Dawson
Publikováno v:
IEEE Transactions on Nuclear Science. 32:711-715
Large area planar drift chambers with long drift distances (up to 50 cm) have been developed for possible use in the new Soudan 2 nucleon decay detector. Design goals included fine sampling to determine the topology of complex events with several low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8646fae205895b837880e7ce0504f308
https://doi.org/10.1109/tns.1985.4336927
https://doi.org/10.1109/tns.1985.4336927
Publikováno v:
Ultrafast Phenomena VI ISBN: 9783642836466
Ultrafast Phenomena VI
Ultrafast Phenomena VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b419ac5443fc16354730fbf2cd43e5e
https://doi.org/10.1007/978-3-642-83644-2_34
https://doi.org/10.1007/978-3-642-83644-2_34
Autor:
S. A. COX, J. ATTWOOD, S. P. BRYANT, R. BAINS, S. POVEY, M. REBELLO, M. KAPSETAKI, N. K. MOSCHONAS, K.-H. GRZESCHIK, M. OTTO, M. DIXON, H. E. SUDWORTH, R. F. KOOY, A. WRIGHT, P. TEAGUE, L. TERRENATO, G. VERGNAUD, S. MONFOUILLOUX, J. WEISSENBACH, O. ALIBERT, C. DIB, S. FAURÉ, E. BARKER, N. M. PEARSON, R. H. A. M. VOSSEN, A. GAL, B. MUELLER-MYHSOK, H. M. CANN, N. K. SPURR
Publikováno v:
Scopus-Elsevier
Annals of Human Genetics, 60, 447-486. Wiley
Annals of Human Genetics, 60, 447-486. Wiley
Meiotic breakpoint panels for human chromosomes 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15, 17, 18, 20 and X were constructed from genotypes from the CEPH reference families. Each recombinant chromosome included has a breakpoint well-supported with refer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afda11e76b1e6bc492579cfbda057c3
http://www.scopus.com/inward/record.url?eid=2-s2.0-12644260443&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-12644260443&partnerID=MN8TOARS