Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sushant, Vinarkar"'
Autor:
Pratiksha Chheda, Shailesh Pande, Tavisha Dama, Sushant Vinarkar, Milind Chanekar, Shweta Limaye, Nilesh Shah, Kirti Chadha
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 32-41 (2020)
Introduction: There is a growing need for BRCA1/BRCA2 mutation frequencies among hereditary breast and ovarian carcinoma (HBOC) cases, specifically determined on the grounds of personal and family history profiles in the Indian population. The curren
Externí odkaz:
https://doaj.org/article/c3d2281013cc474b8d8d3b8a24af8fd3
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 4, Pp GD04-GD06 (2021)
Rett syndrome is an X-linked dominant disorder that is primarily seen in females and is linked to mutations in the gene coding for Methyl-CpG Binding Protein 2 (MeCP2). It is a neurodevelopmental disorder characterised by impairments in language, re
Externí odkaz:
https://doaj.org/article/02fbc20b71fc4fb1a68316420e815c7e
Autor:
Vinay Anand Guntiboina, Vivek S. Radhakrishnan, Jeevan Kumar, Saurabh J. Bhave, Sushant Vinarkar, Jayanta Das, Indu Arun, Deepak Kumar Mishra, Mammen Chandy, Reena Nair
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:780-784
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 2, Pp 379-380 (2020)
Externí odkaz:
https://doaj.org/article/e1b6a7544d6c4c198629490787079bde
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 154-155 (2020)
Externí odkaz:
https://doaj.org/article/7fb17ca924df419d874aabd9461f12ec
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 140-141 (2020)
Externí odkaz:
https://doaj.org/article/c97287dcb7834bc48125ddf3a0dd970a
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 4, Pp 562-564 (2017)
Small cell variant of medullary thyroid carcinoma (MTC) is a rare variant. In the past, primary thyroid lymphomas were thought to be small cell MTC (SCMTC). However, with the advent of immunohistochemistry, it was realized that SCMTC is rare. Our pat
Externí odkaz:
https://doaj.org/article/7dbb1bd94a794299aa9712bd89395c54
Autor:
Milind Chanekar, Kirti Chadha, Shailesh Pande, Pratiksha Chheda, Tavisha Dama, Nilesh Shah, Shweta Limaye, Sushant Vinarkar
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 1, Pp 32-41 (2020)
Introduction: There is a growing need for BRCA1/BRCA2 mutation frequencies among hereditary breast and ovarian carcinoma (HBOC) cases, specifically determined on the grounds of personal and family history profiles in the Indian population. The curren
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 4, Pp GD04-GD06 (2021)
Rett syndrome is an X-linked dominant disorder that is primarily seen in females and is linked to mutations in the gene coding for Methyl-CpG Binding Protein 2 (MECP2). It is a neurodevelopmental disorder characterised by impairments in language, rep
Publikováno v:
Neurology India. 70:1615
Oftentimes, a variation at the multiplex ligation-dependent probe amplification (MLPA) probe binding site leads to improper hybridrization/ligation of the probe showing up as a deletion of an exon leading to false positive results for the detection o