Zobrazeno 1 - 10
of 115
pro vyhledávání: '"M.S. Schanfield"'
Autor:
M.S. Schanfield, H.H. Fudenberg
Publikováno v:
Vox Sanguinis. 26:133-140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40e17b297326d922b462ffff0ef57a33
https://doi.org/10.1159/000467740
https://doi.org/10.1159/000467740
Autor:
Earl J. Brewer, Holly H. Birdsall, Roger D. Rossen, M.S. Schanfield, R.E. Ferrell, Edmond J. Yunis, R.M. Sharp, J. W. Templeton
Publikováno v:
Human Immunology. 4:183-196
Segregation of chromosome #6 markers has been studied in a large family, identified by a proband with seronegative, juvenile-onset rheumatoid arthritis, which contains four individuals with adult-onset rheumatoid arthritis (RA). Two of the adult-onse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f72d5f28907f531b99694866339aa8e
https://doi.org/10.1016/0198-8859(82)90034-9
https://doi.org/10.1016/0198-8859(82)90034-9
Publikováno v:
Human Heredity. 30:343-349
The results of immunoglobulin typing of 268 Tuvinians for G1m (f, z, a, and x), G3m (b, 0, 1, 3, 5, c3, 5, g, s, t and v), A2m (1 and 2) and Km (1) indicate these southern Siberians to have the Caucasian haplotype Gmf; bAm1 (0.100), the Oriental hapl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64d2c49527797a652e40e3ea48a4adc6
https://doi.org/10.1159/000153155
https://doi.org/10.1159/000153155
Autor:
M.S. Schanfield
Publikováno v:
Journal of Human Evolution. 6:341-352
In Australia the distribution of the Gm-Am haplotypes divides the population into two groups. The Western Desert and Central Distriet are characterized by the lack of Gmza;b, while the northern coastal areas are characterized by variable frequenciea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cd1804ca60b5269c9c5eb6bb8dd636f
https://doi.org/10.1016/s0047-2484(77)80003-1
https://doi.org/10.1016/s0047-2484(77)80003-1
Autor:
Urairat Kongmuang, Barbara M. Harpel, M.S. Schanfield, E.A. Azen, Somchai Viriyayudhakorn, Chatchai Klaisuvan, Penjun Bumrungtrakul, Alfred Arnason, R.D. Friedman, Chris C. Plato, P. Veerraju, P.A. Green, Boontaum Khoprasert, Chrysso Plato, Wladimir Wertelecki, M.H. Crawford, Aldur W. Eriksson, Maria Hilling, Malida Pornpatkul, Compee Jitjai, K. Fried, H. Walter, Piyarat Surapruk, R.C. Karn, Olafur Jensson, P.L. Yu, T.E. Alexeyeva, A.D. Merritt, C.S. Chung, Friedrich Kueppers, Rune R. Frants, Prasit Ruengrairatanaroje, Vicharn Panich, Stefan Karlsson, C.L. Carter, S. Micle, Pimpawan Maneechai, Sineenart Kamolmatayakul
Publikováno v:
Human Heredity. 30:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb49ac64160035990c3b44253a45487a
https://doi.org/10.1159/000153153
https://doi.org/10.1159/000153153
Publikováno v:
Human Heredity. 25:370-377
The distribution of G1m(f, z, a, and x), G2m(n), G3m(b0, b1, b3, b5, c3, c5, g, s, t, and v), A2m(1 and 2) and Km(1) (formerly Inv[1]) allotypic determinants has been examined in a series of Czechoslovakian blood donors. The results indicate that Gmz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f46838bb6a581e883d7a946c1a8c2885
https://doi.org/10.1159/000152748
https://doi.org/10.1159/000152748
Autor:
A. Warlow, M. Lahav, H. Sørensen, N.D. Carter, G. Tusnady, J. Dissing, C. Ropartz, L.C. Legueult, I. Persson, K. Ohkura, L. Rivat, G. Beckman, K. Berg, H. Gershowitz, M.S. Adams, T.M. Allan, N. Myrberg, A. Pellicer, D.P. Agarwal, V. Bhalla, James J. Nora, S. Singh, J. Lund, G. Berlin, H.R. Maricq, K. Kølendorf, Anil K. Sinha, L. Beckman, Luan Eng Lie-Injo, Liliane Rivat, S.S. Magnússon, S. Ashbel, L. Kølendorf, L.R. Weitkamp, P.H. Alsbirk, A.W. Eriksson, P.T. Rowley, E. Monn, M.S. Schanfield, B. Sela, B. Bonné, Benkmann Hg, H. Walter, A. Szeinberg, H.-G. Benkmann, K.E. Alsbirk, Q.B. Welch, A. Czeizel, A.R. Coward, L. Hirth, Sen Pathak, Hazel Camoens, A.E. Mourant, C.J. Brackenridge, T. Pellicer, T.E.B. Leakey, P.Y. Rousseau, H. Arvilommi, R. Ananthakrishnan, M. Stahn, H.W. Goedde, L. Tsacheva
Publikováno v:
Human Heredity. 22:I-VIII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef0aa8639bddcd930834e78f3cfbd341
https://doi.org/10.1159/000152517
https://doi.org/10.1159/000152517
Publikováno v:
Human Heredity. 22:144-148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a2c9347e78ed70cbc9ebed89f5f4231
https://doi.org/10.1159/000152482
https://doi.org/10.1159/000152482
Akademický článek
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Akademický článek
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