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Measurement of the muon neutrino charged-current single π + production on hydrocarbon using the T2K off-axis near detector ND280

Autor: K. Abe, R. Akutsu, A. Ali, C. Alt, J. Amey, C. Andreopoulos, L. Anthony, M. Antonova, S. Aoki, A. Ariga, Y. Ashida, E. T. Atkin, Y. Awataguchi, Y. Azuma, S. Ban, M. Barbi, G. J. Barker, G. Barr, C. Barry, M. Batkiewicz-Kwasniak, A. Beloshapkin, F. Bench, V. Berardi, S. Berkman, R. M. Berner, L. Berns, S. Bhadra, S. Bienstock, A. Blondel, S. Bolognesi, S. Bordoni, B. Bourguille, S. B. Boyd

Publikováno v: Physical Review D

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::92c5ad0c445df288144b0640a9575b38

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Autor: Werner Schempp, G. Wöhr, Ingrid Eisenbarth, Günter Assum, Barbi G, Hildegard Kehrer-Sawatzki

Publikováno v: Chromosome Research. 6:429-435

Members of the long-range, low-copy-number repetitive DNA sequence family chAB4 are located on nine different human chromosome pairs and the Y chromosome, i.e. on the short arms of all the acrocentrics. To localize the chAB4 sequences more precisely

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8630929f131c708edd6677dd86eeb738
https://doi.org/10.1023/a:1009287223826

An excess of chromosome 1 breakpoints in male infertility

Autor: Bache, I., Van Assche, E., Cingoz, S., Bugge, M., Tümer, Z., Hjorth, M., Lundsteen, C., Lespinasse, J., Winther, K., Niebuhr, A., Kalscheuer, V., Liebaers, I., Bonduelle, M., Tournaye, H., Ayuso, C., Barbi, G., Blennow, E., Bourrouillou, G., Brondum-Nielsen, K., Bruun-Petersen, Gert, Croquette, M.F., Dahoun, S., Dallapiccola, B., Davison, V., Delobel, B., Duba, H.C., Duprez, L., Ferguson-Smith, M., FitzPatrick, D.R., Grace, E., Hansmann, I., Hultén, M., Jensen, P.K.A., Jonveaux, P., Kristoffersson, U., Lopez-Pajares, I., McGowan-Jordan, J., Murken, J., Orera, M., Parkin, T., Passarge, E., Ramos, C., Rasmussen, Kirsten

Publikováno v: Bache, I, Van Assche, E, Cingoz, S, Bugge, M, Tümer, Z, Hjorth, M, Lundsteen, C, Lespinasse, J, Winther, K, Niebuhr, A, Kalscheuer, V, Liebaers, I, Bonduelle, M, Tournaye, H, Ayuso, C, Barbi, G, Blennow, E, Bourrouillou, G, Brondum-Nielsen, K, Bruun-Petersen, G, Croquette, M F, Dahoun, S, Dallapiccola, B, Davison, V, Delobel, B, Duba, H C, Duprez, L, Ferguson-Smith, M, FitzPatrick, D R, Grace, E, Hansmann, I, Hultén, M, Jensen, P K A, Jonveaux, P, Kristoffersson, U, Lopez-Pajares, I, McGowan-Jordan, J, Murken, J, Orera, M, Parkin, T, Passarge, E, Ramos, C & Rasmussen, K 2004, ' An excess of chromosome 1 breakpoints in male infertility. ', European Journal of Human Genetics, vol. 12, pp. 993-1000 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3062::5a374fae6724147fb3cbe4c18c19b89e
https://portal.findresearcher.sdu.dk/da/publications/14fe6160-f198-11db-821c-000ea68e967b

COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - ONE-YEAR PROGRESS REPORT

Autor: Sherman, Sl, Barbi, G, Brondumnielsen, K, Brown, Wt, Carpenter, Nj, Chudley, Ae, Ferraz, Op, Ferreira, P, Gustavson, Kh, Halliday, J, Hockey, A, Howardpeebles, Pn, Jenkins, E, Kennerknecht, I, Kahkonen, M, Ladaique, P, Leisti, J, Maddalena, A, Mazurczak, T, Mattei, Jf, Mattina, Teresa, Mckinley, Mj, Murphy, P, Pellissier, Mc, Purvissmith, S, Robinson, H, Scapagnini, U, Schaap, T, Shapiro, Lr, Smits, Apt, Steinbach, P, Turner, G, Uchida, Ia, Vanoost, Ba, Voelckel, Ma, Weaver, Dd, Webb, T.

Publikováno v: American Journal of Medical Genetics, 43(1-2), 355-360. WILEY-LISS

A prospective study of the fragile X syndrome [fra(X)] was initiated one year ago to refine the estimates of recurrence risks based on the phenotype of the mother and the family history of the syndrome. The basic unit of data consists of the descript

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::144d157b1b84fb9a488b7242bee7a264
https://research.rug.nl/en/publications/05008372-5464-4633-aa20-acf1a87ed10c