Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yogita Salunkhe"'
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
Autor:
Milind Chanekar, Anurita Pais, Pratiksha Chheda, Rajesh Bendre, Yogita Salunkhe, Nilesh Shah, Tavisha Dama, Shailesh Pande
Publikováno v:
Molecular Diagnosis & Therapy. 22:353-359
Huntington’s disease (HD) is an autosomal-dominant neurodegenerative disorder with an average age at onset of 40 years. It is a polyglutamine (polyQ) disorder that is caused by an increase in the number of CAG repeats in the huntingtin (HTT) gene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::500b96825a2001078620555b5886518e
https://doi.org/10.1007/s40291-018-0327-y
https://doi.org/10.1007/s40291-018-0327-y
Autor:
Jyothi Britto, Nilesh Shah, Yogita Salunkhe, Tejaswi Dalvi, Milind Chanekar, Reshma Haryan, Pratiksha Chheda, Rajesh Bendre, Sandeep Warghade, Sunmeet Matkar
Publikováno v:
Journal of Laboratory Physicians
Journal of Laboratory Physicians, Vol 10, Iss 01, Pp 073-079 (2018)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d66231a43cdeee2f579cba00c3f8116
https://doi.org/10.4103/jlp.jlp_57_17
https://doi.org/10.4103/jlp.jlp_57_17
Autor:
Anurita Pais, Shailesh Pande, Sunmeet Matkar, Pratiksha Chheda, Nitin Choubal, Yogita Salunkhe, Ashish Parulekar
Publikováno v:
International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 6:2631
Triploidy is a complete extra set of chromosomes. In the current case report, we present the case of a 29-year-old pregnant female who was referred to Department of Genetics, Metropolis Healthcare Ltd, Mumbai. Real-time sonography of the gravid uteru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4144a335e79c74662ade9358eefe7b2
https://doi.org/10.18203/2320-1770.ijrcog20172368
https://doi.org/10.18203/2320-1770.ijrcog20172368