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All samples we confirmed to have normal karyotypes using standard cytogenetic techniques.
These deletions are difficult to visualize using standard cytogenetic techniques.
The cells were harvested and the slides prepared using standard cytogenetic techniques.
The cell cultures were harvested and chromosome preparations were made using standard cytogenetic techniques.
Karyotypes were determined using standard cytogenetic techniques and described according to the International System for Human Cytogenetic Nomenclature (ISCN 2009).
Metaphase cells were prepared using standard cytogenetic techniques, and air-dried slides were prepared and stained using Trypsin Giemsa banding techniques as described previously (35).
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Using standard cytogenetic technique, lymphocyte cultures were prepared with all samples.
Metaphase cells were obtained using standard cytogenetic methods.
Conventional cytogenetic G-Banding analysis was carried out on all samples included in this study (CV, amniotic fluid, foetal blood, and skin) using standard cytogenetic methodologies [ 11].
Peripheral blood lymphocytes were processed using standard clinical cytogenetic techniques.
Standard cytogenetic techniques were used to prepare and stain chromosome spreads [37], [52].
More suggestions(15)
using standard diagnostic techniques
using standard cytogenetic protocols
using standard analytical techniques
using conventional cytogenetic techniques
using established cytogenetic techniques
using standard parametric techniques
using different cytogenetic techniques
using standard molecular techniques
using current cytogenetic techniques
using standard cytogenetic packets
using standard cytogenetic methods
using traditional cytogenetic techniques
using standard immunohistochemical techniques
using standard histological techniques
using standard microbiological techniques
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