Je was op zoek naar: karyotype (Deens - Engels)

karyotype
karyotype

bestemmelse af fosterets karyotype
foetal karyotyping

før behandlingen bør der udføres komplet blodstatus med differentialtælling og trombocyttal samt evaluering af knoglemarvsmorfologi og karyotype.
complete blood cell counts with differential and platelet counts and an evaluation of bone marrow morphology and karyotype should be performed prior to treatment.

der bør foretages fuldstændige blodcelletællinger med differentialtælling og trombocyttal samt evaluering af knoglemarvsmorfologi og karyotype, inden behandlingen igangsættes.
complete blood cell counts with differential and platelet counts, and an evaluation of bone marrow morphology and karyotype should be performed prior to treatment.

før behandlingen bør der foretages fuldstændig blodcelletælling, herunder differentialtælling og trombocyttælling, og knoglemarvsmorfologi og karyotype bør evalueres før behandlingen.
complete blood cell counts with differential and platelet counts, and an evaluation of bone marrow morphology and karyotype should be performed prior to treatment.

før behandlingen bør der foretages en fuldstændig blodcelletælling med differential- og trombocyttælling, og der bør udføres en evaluering af knoglemarvsmorfologi og karyotype.
complete blood cell counts with differential and platelet counts and an evaluation of bone marrow morphology and karyotype should be performed prior to treatment.

der observeredes en tendens til forbedret pfs hos patienter med 17 q deletion, trisomi 12 og normal karyotype, som ikke nåede signifikans på grund af den lille populationsstørrelse.
a trend towards improved pfs was observed in patients with 17p deletion, trisomy 12 and normal karyotype, which did not reach significance due to small sample size.

hos førstegangsbehandlede patienter behandlet med enten campath eller chlorambucil var der 21 patienter med 17 q deletion, 54 patienter med 11 q deletion, 34 patienter med trisomi 12, 51 patienter med normal karyotype og 67 patienter med kun 13 q deletion.
in first line patients, treated with either campath or chlorambucil, there were there were 21 patients with the 17p deletion, 54 patients with 11q deletion, 34 patients with trisomy 12, 51 patients with normal karyotype and 67 patients with sole 13q deletion.

ud af de 1. linje-patienter (n=282) hos hvem der var cytogene (fish) data til rådighed ved udgangspunktet i undersøgelse 4, blev der detekteret kromosomale afvigelser hos 82%, mens normal karyotype blev detekteret hos 18%.
of the first-line patients (n=282) in whom baseline cytogenetic (fish) data were available in study 4, chromosomal aberrations were detected in 82%, while normal karyotype was detected in 18%.