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The phrase "abnormality in three" is grammatically correct and can be used in written English.
It can be used in contexts where you are discussing a specific abnormality that is related to the number three, such as in a medical, statistical, or analytical context.
Example: "The study revealed an abnormality in three of the test subjects, indicating a potential pattern that requires further investigation."
Alternatives: "irregularity in three" or "anomaly in three".
Exact(2)
Ten patients (13%) had only one abnormality in their PCs, and for these, BM-lymphocytes had the same abnormality in three of them (30%).
The colposcopic evaluation of all five TCA cases excluded any cervical abnormality in three women with normal or borderline Pap smears.
Similar(58)
Mammography failed to identify an abnormality in four patients (24%%), presumably due to overlapping dense breast parenchyma obscuring potential findings.
Likewise, amplification of the 14q32 was detected in 23 (14%) patients with BM-lymphocytes bearing the same abnormality in two (9%) of them.
T2w-MRC diagnosed the abnormality in six (40%%) of these patients, whereas combined T2w-MRC and CE-MRC images detected the abnormality in 12 patients (80%%; P < 0.05; Fig. 3a, c).
Moreover, in 46 subjects with IGT, an abnormality in four of five cardiovascular reflex tests, a greater heart rate variability, and increased heat detection thresholds have been shown recently (16).
Combined routine T2w-MRC and CE-MRC images achieved to demonstrate extravasation in 11 of these patients (84.6 %; P < 0.05), whereas T2w-MRC failed to identify the abnormality in seven patients (false-negative rate, 53.8 %; Fig. 1a-c).
Multivariate linear regression analysis was used to identify independent contributions of site ischaemia (diffusion and/or perfusion abnormality in seven Brodmann areas in language cortex), age, total volume of infarct (on diffusion-weighted imaging), and total volume of hypoperfusion (on perfusion-weighted imaging).
Louwette et al. now characterise platelet abnormalities in three unrelated patients carrying NPC1 mutations, and in NPC1-depleted zebrafish embryos.
This review highlights investigations that showed urothelial abnormalities in three functional bladder conditions: BPS/IC, FIC, and OAB.
Germline mutations of the PTPN11 gene also cause skeletal abnormalities in three distinct autosomal-dominant human diseases.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com