Zobrazeno 1 - 10
of 100
pro vyhledávání: '"G. Bruun Petersen"'
Publikováno v:
Hereditas. 85:157-162
The Swedish moose (Alces alces) population was chosen as a model for the estimation of the effects of selective hunting policies on the genetic structure of a population. The need for genetic markers led us to initiate an electrophoretic examination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cd2f29d168ec1966c254543d16b5555
https://doi.org/10.1111/j.1601-5223.1977.tb00963.x
https://doi.org/10.1111/j.1601-5223.1977.tb00963.x
Autor:
P. Platz, A. Svejgaard, L. P. Ryder, Niels Morling, Bodil K. Jakobsen, L. U. Lamm, Tom Kristensen, G Bruun-Petersen
Publikováno v:
Tissue Antigens. 22:123-133
The chromosome 6 markers, HLA-ABC, D, DR, MT, properdin factor Bf, and complement factors 2 (C2) and 5 (C4), were studied in three families, each of which included two HLA identical siblings, one or both of whom were known to be HLA-B: GLO recombinan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::452f7e6a1d12f27f833ba0674bdb06fa
https://doi.org/10.1111/j.1399-0039.1983.tb01178.x
https://doi.org/10.1111/j.1399-0039.1983.tb01178.x
Autor:
Erik Thorsby, F. Kissmeyer-Nielsen, L. U. Lamm, Arne Svejgaard, G. Högman, G. Bruun Petersen, Wolfgang R. Mayr
Publikováno v:
Tissue Antigens. 2:205-214
A study of four families with a cross-over within the HL—A region and in which the crossover parent is heterozygous at PGM3 indicates with a probability of about 95% that the chromosomal orientation of the three linked loci is LA · FOUR · PGM3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69e0a288b4e6dad01bdb241fd989e202
https://doi.org/10.1111/j.1399-0039.1972.tb00137.x
https://doi.org/10.1111/j.1399-0039.1972.tb00137.x
Publikováno v:
Clinical Genetics. 26:265-268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d7f212b0bb6672e98028dbf1eec06ea
https://doi.org/10.1111/j.1399-0004.1984.tb04388.x
https://doi.org/10.1111/j.1399-0004.1984.tb04388.x
Autor:
Åge J. Therkelsen, U. Merrild, K. Kristoffersen, I. Hägerstrand, M. Hauge, Bent Nørgaard-Pedersen, G. Bruun Petersen, Ursula Friedrich, E. Ludvigsen, K. Brogård Hansen
Publikováno v:
Clinical Genetics. 15:278-286
Two unrelated families are presented with repeated occurrences of a congenital syndrome of which the main stigmata were polycystic kidneys and occipital encephalocele (Meckel syndrome). Prenatal diagnosis, followed by interruption of pregnancy, was p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91c16c3d1b58583f4ca51385938f6208
https://doi.org/10.1111/j.1399-0004.1979.tb00980.x
https://doi.org/10.1111/j.1399-0004.1979.tb00980.x
Autor:
Steen Kølvraa, Cássio van den Berg, G. Bruun-Petersen, D. G. Crüger, S Ziebe, C Hnida, Inge Agerholm
Publikováno v:
Agerholm, I E, Hnida, C, Crüger, D G, Berg, C, Bruun-Petersen, G, Kølvraa, S & Ziebe, S 2008, ' Nuclei size in relation to nuclear status and aneuploidy rate for 13 chromosomes in donated four cells embryos ', Journal of Assisted Reproduction and Genetics, vol. 25, no. 2-3, pp. 95-102 . https://doi.org/10.1007/s10815-008-9199-0
Udgivelsesdato: null-null PURPOSE: The aim was to elucidate if the nuclear size and number are indicative of aberrant chromosome content in human blastomeres and embryos. METHODS: The number of nuclei and the nucleus and blastomere size were measured
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4ee33028a09b2cce7e243f7de4ab8f
https://doi.org/10.1007/s10815-008-9199-0
https://doi.org/10.1007/s10815-008-9199-0
Publikováno v:
Clinical Genetics. 64:198-203
A total of 392 men referred for intracytoplasmic sperm injection (ICSI) participated in genetic analysis. The control group consisted of 100 normal fertile males. Chromosome and DNA analyses were performed to investigate the frequency of Y-chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d62dfba3a05a78300f813cf6c7546c50
https://doi.org/10.1034/j.1399-0004.2003.00128.x
https://doi.org/10.1034/j.1399-0004.2003.00128.x
Autor:
P. Giannini, Nurdan Uras, Nilufer Guzoglu, D. Wunder, V. Bianchi, C. Piscitelli, Mona Oudi, G. Bruun-Petersen, Andrea Borini, Hayriye Gozde Kanmaz, Raffaella Sciajno, R.P. Cotarelo, Monica Cattoli, M. Lappi, E. Antinori, P. Rubino, B. Bay, Ermanno Greco, M.A Bonu, M. Bellavia, Ugur Dilmen, Alessandra Alteri, A. Colicchia, R. Omani Samani, Dilek Dilli, Omer Erdeve
Publikováno v:
Human Reproduction. 27:ii224-ii226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60f4d82ce8865ab6418cef333a405f56
https://doi.org/10.1093/humrep/27.s2.79
https://doi.org/10.1093/humrep/27.s2.79
Publikováno v:
Clinical Genetics. 61:35-39
The aim of the investigation was to study fertility in Danish women diagnosed with Turner syndrome (TS), and to describe their offspring. In total, 410 women in the fertile age were registered in the Danish Cytogenetic Central Register with TS betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::214f24a659aabab0b2378933a490b7a0
https://doi.org/10.1034/j.1399-0004.2002.610107.x
https://doi.org/10.1034/j.1399-0004.2002.610107.x
Publikováno v:
Prenatal Diagnosis. 17:635-642
Uncultured coelomic cells were hybridized with alpha satellite DNA probes representing chromosomes X, Y, 18, and 13/21 in order to evaluate the distribution of hybridization signals obtained by fluorescence in situ-hybridization (FISH) analysis of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9bf122230235801b20fcb36865a14c2
https://doi.org/10.1002/(sici)1097-0223(199707)17:7<635::aid-pd127>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199707)17:7<635::aid-pd127>3.0.co