Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Dutta, Usha R"'
Autor:
Dutta, Usha R., Rao, Sudha N., Pidugu, Vijaya Kumar, V.S., Vineeth, Bhattacherjee, Amrita, Bhowmik, Aneek Das, Ramaswamy, Sathish K., Singh, Kumar Gautam, Dalal, Ashwin
Publikováno v:
In Genomics September 2019 111(5):1108-1114
Publikováno v:
In European Journal of Medical Genetics March 2015 58(3):154-159
Autor:
Dutta, Usha R.1 (AUTHOR) usha@cdfd.org.in, Suttur, Malini S.2 (AUTHOR), Venugopal, Vineeth S.1 (AUTHOR), Posanapally, Laxmi Priyanka1 (AUTHOR), Gopalasetty, Sravani1 (AUTHOR), Talwar, Sangamesh2 (AUTHOR), Anand, Suhana2 (AUTHOR), Billapati, Sushmita1 (AUTHOR), Jesudasan, Rachel A.3 (AUTHOR), Dalal, Ashwin1 (AUTHOR)
Publikováno v:
Andrologia. Nov2020, Vol. 52 Issue 10, p1-9. 9p.
Autor:
Dutta, Usha R., Bhattacherjee, Amrita, Bahal, Ashish, Posanapally, Laxmi P., Lone, Kaisar A., Bathula, Siddardha, Dalal, Ashwin
Publikováno v:
Mol Syndromol
INTRODUCTION: The accurate detection of breakpoint regions of disease-associated chromosomal rearrangements helps understand the molecular mechanisms and identify the risks involved with disrupted genes. METHODS: In this study, a girl with growth ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::132585b5a15275c88a1c3e47147854f3
https://europepmc.org/articles/PMC9801327/
https://europepmc.org/articles/PMC9801327/
Autor:
Dutta, Usha R.1 usha@cdfd.org.in, Swamy, Venugopala1, Ponnala, Rajitha1, Aggarwal, Shagun1,2, Dalal, Ashwin1
Publikováno v:
Journal of Reproduction & Infertility. Apr-Jun2019, Vol. 20 Issue 2, p109-114. 6p. 2 Color Photographs, 1 Black and White Photograph, 1 Diagram.
Autor:
Dutta, Usha R., Bahal, Ashish, Vineeth, V.S., Sarvade, Vasantha, Ranganath, Prajnya, Dalal, Ashwin
Publikováno v:
In Gene Reports September 2017 8:128-133
Publikováno v:
Journal of Reproduction & Infertility. Apr-Jun2014, Vol. 15 Issue 2, p113-116. 4p. 3 Diagrams.
Autor:
Alber, Michael, Kalscheuer, Vera M., Marco, Elysa, Sherr, Elliott, Lesca, Gaetan, Till, Marianne, Gradek, Gyri, Wiesener, Antje, Korenke, Christoph, Mercier, Sandra, Becker, Felicitas, Yamamoto, Toshiyuki, Scherer, Stephen W., Marshall, Christian R., Walker, Susan, Dutta, Usha R., Dalal, Ashwin B., Suckow, Vanessa, Jamali, Payman, Kahrizi, Kimia, Najmabadi, Hossein, Minassian, Berge A.
Publikováno v:
Neurology: Genetics
Objective: We aimed to generate a review and description of the phenotypic and genotypic spectra of ARHGEF9 mutations. Methods: Patients with mutations or chromosomal disruptions affecting ARHGEF9 were identified through our clinics and review of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0699646694f9dc3b7d0de4f3cb19f872
http://europepmc.org/articles/PMC5446782
http://europepmc.org/articles/PMC5446782
Autor:
Dutta, Usha R.1 ushadutta@hotmail.com, Ponnala, Rajitha1, Pidugu, Vijaya Kumar1, Dalal, Ashwin B.1
Publikováno v:
Archives of Iranian Medicine (AIM). May2013, Vol. 16 Issue 5, p267-270. 4p.
Publikováno v:
Case Reports in Genetics. 2012, p1-5. 5p.