In our study, single gene deletions
were predominantly found and seems attributable to the findings in previous studies which mentioned that a single [alpha] gene deletion
does not produce a significant ameliorating effect in [beta]0-thalassemia.This form was mostly prevalent in our cohort.
The letter further stated that such deletions
were reported to the Election Commission during the Vidhan Sabha elections too but no action was taken.
700,000 applications were received by the officials all over the state for the deletion
of voters' names and an investigation was conducted by the authorities to identify the persons responsible for submitting these forms.
Peru and recently Eritrea had a high percentage of gene deletion
and so a high percentage of false negatives.
Chairman of the committee observed that all the projects have certain public significance and their deletion
from the list would add to the hardships of the people, however, the mechanism adopted by the ministry concerned is ambiguous and there is need to adopt a holistic approach to prioritise the development plans as per public needs.
Lacson recalled that he also asked for the deletion
of the P50 billion ROW funding in the 2018 budget.
We looked for a 22q11.2 deletion
in 39 Mexican patients with craniofacial dysmorphisms suggestive of DGS or VCFS and at least one major phenotypic feature, namely cardiac anomaly, immune deficiency, palatal defects or development delay (1).
Table-I: Frequency distribution and odds ratio (95% CI) of GSTM1 and GSTT1 deletion
among ALL patients and controls.
Eighteen pairs of multiplex PCR primers covering exons in the deletion
hotspots were divided into two groups to amplify: one encompasses exons 4, 8, 12, 17, 19, 44, 45, 48, and 51 and the other encompasses promoter and exons 3, 6, 13, 43, 47, 50, 52, and 60.
A bizarre game of hide-and-seek took place through "The Land of Obsolete Men" leading into "The Dome of Deletion
of the 11p15.4 region is associated with autosomal dominant hereditary persistence thalassemia (HPFH, OMIM: 141749) and autosomal recessive beta-thalassemia (OMIM: 141900) [11, 12].
In the genetic study, we identified a deletion
of 7.23 Mb in the 7p13-p12.1 region (genomic coordinates Chr7: 42807167 to 50040279).