Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Pratiksha Chheda"'
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:
Sandeep Warghade, Jyothi Britto, Reshma Haryan, Tejaswi Dalvi, Rajesh Bendre, Pratiksha Chheda, Sunmeet Matkar, Yogita Salunkhe, Milind Chanekar, Nilesh Shah
Publikováno v:
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
CONTEXT: Hemoglobinopathies constitute the world's most common genetically inherited red blood cell disorder. Screening and accurate identification of hemoglobin (Hb) variants have become increasingly important in antenatal diagnosis and prevention o
Externí odkaz:
https://doaj.org/article/ae7f33f43a934fe9aed25c811dd49911
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
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:
Archives of Clinical and Medical Case Reports.
Autor:
Bagwan Jamir, Pratiksha Chheda, Bhalerao Rahul, Bhat Devdatta, Dama Tavisha, Shashikala Shivaprakash
Rapid diagnostic tests are of great importance in hospital settings during the current outbreak of SARS-CoV-2. The clinical patient management and spread of infection is critically dependent on molecular assays with shortest possible turn-around time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a58fb50155ffa2ce1e0a76eac95f0e31
https://doi.org/10.21203/rs.3.rs-731426/v1
https://doi.org/10.21203/rs.3.rs-731426/v1
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