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Comprehensive analysis of genetic factors predicting overall survival in Myelodysplastic syndromes.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09864-9
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- Article
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
- Published in:
- Molecular Human Reproduction, 2023, v. 29, n. 2, p. 1, doi. 10.1093/molehr/gaad001
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- Publication type:
- Article
Correction to: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-021-01152-1
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- Publication type:
- Article
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-021-01152-1
- By:
- Publication type:
- Article
Lack of association between functional polymorphism of DNA repair genes (XRCC1, XPD) and clinical response in Indian chronic myeloid leukemia patients.
- Published in:
- Molecular Biology Reports, 2019, v. 46, n. 5, p. 4997, doi. 10.1007/s11033-019-04950-0
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- Publication type:
- Article
Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective study.
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- Journal of Cancer Research & Therapeutics, 2023, v. 19, n. 2, p. 340, doi. 10.4103/jcrt.jcrt_393_22
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- Publication type:
- Article
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 3, p. 2519, doi. 10.1007/s11033-021-06293-1
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- Publication type:
- Article
Severe telomere shortening in Fanconi anemia complementation group L.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 1, p. 585, doi. 10.1007/s11033-020-06101-2
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- Publication type:
- Article
Comprehensive Study of Chromosomal Copy Number Variations and Genomic Variations Predicting Overall Survival in Myelodysplastic Syndromes.
- Published in:
- Oncology, 2024, v. 102, n. 10, p. 897, doi. 10.1159/000536446
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- Publication type:
- Article
Chromosomal Aberrations in Primary Amenorrhea: A Retrospective Study.
- Published in:
- Journal of Human Reproductive Sciences, 2019, v. 12, n. 2, p. 92, doi. 10.4103/jhrs.JHRS_107_16
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- Publication type:
- Article