Items where Author is "Komachali, S. R."

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Number of items: 6.

Article

(2023) CHRNG gene mutations found by whole exome sequencing are related to recurrent pregnancy loss. Human Gene. ISSN 27730441 (ISSN)

(2023) DOK7 Gene Novel Homozygous Mutation is Related to Fetal Akinesia Deformation Sequence 3. Journal of Obstetrics and Gynecology of India. pp. 222-226. ISSN 0971-9202

(2022) Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran. Genomics & informatics. e30. ISSN 1598-866X (Print) 2234-0742 (Electronic) 1598-866X (Linking)

(2022) An experimental in silico study on COVID-19: Response of neutrophil-related genes to antibiotics. HEALTH SCIENCE REPORTS. ISSN 2398-8835 J9 - HEALTH SCI REP-US

(2022) A novel NR0B1 mutation correlated with X-linked adrenal hypoplasia congenital (AHC). GENE REPORTS. ISSN 2452-0144 J9 - GENE REP

(2022) A novel mutation in GJC2 associated with hypomyelinating leukodystrophy type 2 disorder. Genomics Inform. e24. ISSN 1598-866X (Print) 1598-866x

This list was generated on Thu May 8 19:31:12 2025 +0330.