Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dagmar Kühn"'
Autor:
J. B. Trapp, Dagmar Kühn, A. M. Eckstein, Sarah Byers, J. R. Harrison, Pier Franco Beatrice, Michael Edwards, Ingrid Alexander-Skipnes, Volker Riedel, Carl J. Richard, Jeremy J. Mhire
Publikováno v:
International Journal of the Classical Tradition. 11:456-492
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8d16af06d4a6194c8b4a5e944adbbe
https://doi.org/10.1007/s12138-005-0006-3
https://doi.org/10.1007/s12138-005-0006-3
Autor:
Dagmar Kühn
The great variety of Aramaic dialects in the different kingdoms of the 9th and 8th centuries B.C.10 as well as the lack of archaeological proof of a common Aramaean culture speaks in favour of ethnic diversity among the Aramaeans. Fundamental to trib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db49bbdbaee48ed27e2774fd88b14f9c
https://doi.org/10.1163/9789004229433_004
https://doi.org/10.1163/9789004229433_004
Autor:
Dagmar Kühn
Publikováno v:
Syria. :444-446
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4ffacec7779b65094d2117e0a7b537f
https://doi.org/10.4000/syria.850
https://doi.org/10.4000/syria.850
Publikováno v:
Cancer genetics and cytogenetics. 30(2)
We report on the cytogenetic findings in six cases of acute promyelocytic leukemia, studied in two different cytogenetic laboratories in Germany. A t(15;17) was detected in three cases. This finding reveals that the t(15;17) in acute nonlymphocytic l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b16207a4ee2ea520359791a08907a3e4
https://pubmed.ncbi.nlm.nih.gov/3422585
https://pubmed.ncbi.nlm.nih.gov/3422585
Publikováno v:
Cancer genetics and cytogenetics. 25(1)
En colorant au Giemsa pour la formation de bandes les caryotypes de 24 malades atteints d'une leucemie myeloide chronique Ph + on a decouvert 3 translocations atypiques. Un malade presentait une translocation complexe t(9;12;22)(934;915;911) et deux
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e440269f4ce8f30169eff45894d0f61
https://pubmed.ncbi.nlm.nih.gov/3467828
https://pubmed.ncbi.nlm.nih.gov/3467828
Publikováno v:
Human genetics. 76(4)
Chromosome studies in a phenotypically normal 40-year-old man with Philadelphia (Ph) chromosome-positive chronic myelocytic leukemia (CML) and a constitutional Robertsonian translocation are reported. The possibility of carriers of Robertsonian trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dda38b2b307a5525878fe5782d1f9c51
https://pubmed.ncbi.nlm.nih.gov/3475248
https://pubmed.ncbi.nlm.nih.gov/3475248