[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 23.

Article

Dutta, Usha and Suttur, M.S. and Vineeth, V.S. and Laxmi Priyanka, P. and Sravani, G. and Talwar, S. and Suhana, A. and Sushmita, B. and Rachel, J.A. and Dalal, Ashwin (2020) Cytogenetic and molecular study of 370 infertile men in South India highlighting the importance of copy number variations by multiplex ligation‐dependent probe amplification. Andrologia. ISSN 0303-4569 (In Press)

Dutta, Usha and Rao, S.N. and Vijaya Kumar, P. and Vineeth, V.S. and Bhattacherjee, Amrita and Das Bhowmik, A. and Ramaswamy, S.K. and Singh, K.G. and Dalal, Ashwin (2019) Breakpoint mapping of a novel de novo translocation t(X;20)(q11.1;p13) by positional cloning and long read sequencing. Genomics, 111 (5). pp. 1108-1114. ISSN 0888-7543

Dutta, Usha and Swamy, Venugopala and Rajitha, Ponnala and Aggarwal, Shagun and Dalal, Ashwin (2019) Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS. Journal of Reproduction and Infertility, 20 (2). pp. 109-114. ISSN 2228-5482

Vineeth, V.S. and Dutta, Usha and Karthik, T. and Das Bhowmik, A. and Dalal, Ashwin (2018) Whole exome sequencing identifies a novel 5 Mb deletion at 14q12 region in a patient with global developmental delay, microcephaly and seizures. Gene, 673. pp. 56-60. ISSN 0378-1119

Dutta, Usha and Bahal, Ashish and Vineeth, V.S. and Vasantha, S. and Ranganath, P. and Dalal, Ashwin (2017) A novel mosaic complex supernumerary marker chromosome in a girl with seizures: Systematic characterization of the complex marker. Gene Reports, 8. pp. 128-133. ISSN 2452-0144

Dutta, Usha (2016) The history of Human cytogenetics in India- A review. Gene, 589 (2). pp. 112-117. ISSN 0378-1119

Dutta, Usha and Hansmann, I. and Schlote, D. (2015) Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature. European Journal of Medical Genetics, 58 (3). pp. 154-159. ISSN 1878-0849

Dutta, Usha and Vempally, S. and Ranganath, P. and Dalal, Ashwin (2014) A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker. Gene, 539 (1). pp. 162-7. ISSN 1879-0038

Dutta, Usha and Rajitha, Ponnala and Dalal, Ashwin (2014) A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report. Journal of Reproduction and Infertility, 15 (2). pp. 113-116. ISSN 2251-676X

Dutta, Usha and Vijaya Kumar, P. and Goud, Ch.V. and Hoefers, C. and Hagemann, M. and Dalal, Ashwin (2013) Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development. Gene, 519 (2). pp. 374-380. ISSN 0378-1119

Dutta, Usha and Rajitha, Ponnala and Vijaya Kumar, P. and Dalal, Ashwin (2013) Chromosomal abnormalities in amenorrhea: a retrospective study and review of 637 patients in South India. Archives of Iranian medicine, 16 (5). pp. 267-70. ISSN 1735-3947

Dutta, Usha and Vijaya Kumar, P. and Dalal, Ashwin (2012) Molecular Cytogenetic Characterization of a Non-Robertsonian Dicentric Chromosome 14;19 Identified in a Girl with Short Stature and Amenorrhea. Case Reports in Genetics, 2012. ID 212065. ISSN 2090-6544

Dutta, Usha and Vijaya Kumar, P. and Dalal, Ashwin (2012) Molecular and cytogenetic characterization of two patients with recurrent miscarriages and X-autosome translocation. Journal of Research in Medical sciences, 17 (6). pp. 572-4. ISSN 1735-1995

Rajitha, Ponnala and Ranganath, P. and Dutta, Usha and Pidugu, V.K. and Dalal, Ashwin (2012) Phenotypic and Molecular Characterization of Partial Trisomy 2q Resulting from Insertion-Duplication in Chromosome 18q: A Case Report and Review of Literature. Cytogenetic and Genome Research, 136 (3). pp. 229-234. ISSN 1424-8581

Dutta, Usha and Vijaya Kumar, P. and Goud, Ch.V. and Dalal, Ashwin (2012) Mosaic Down syndrome with a marker: Molecular cytogenetic characterization of the marker chromosome. Gene, 495 (2). pp. 199-204. ISSN 0378-1119

Vineeth, V.S. and Malini, S.S. and Sreenivasa, G. and Dutta, Usha (2012) High incidence of sperm dysfunction in a varicocele infertile man: case report. Asian Pacific Journal of Reproduction, 1 (1). pp. 63-66. ISSN 2305-0500

Vijaya Kumar, P. and Dutta, Usha (2012) Fluorescence in .situ Hybridization: Technology and its application in Molecular Medicine. Journal of Cytology and Genetics, 13 (1-2). pp. 1-8. ISSN 0253-7605

Dutta, Usha and Rajitha, Ponnala and Vijaya Kumar, P. and Dalal, Ashwin (2011) Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review. Journal of Assisted Reproduction and Genetics, 28 (2). pp. 145-149. ISSN 1058-0468

Malini, S.S. and Vijaya Kumar, P. and Dalal, Ashwin and Dutta, Usha (2011) Evaluation of sex chromosomal anomalies in sperms among infertile males by Fluorescence in situ Hybridization. Journal of Cytology and Genetics, 12. pp. 77-84. ISSN 0253-7605

Radha Rama Devi, A. and Dutta, Usha (2011) Ring Chromosome 20 Associated with Refractory Epilepsy: A Case Report. Asian Journal of Medical Sciences, 2 (3). pp. 141-144. ISSN 2091-0576

Prabhakara, K. and Dutta, Usha and Radha Rama Devi, A. (2002) A partial 15q22 trisomy arising due to segregation of maternal 10;15 reciprocal translocation. Indian Pediatrics, 39 (11). pp. 1050-1054. ISSN 0019-6061

Radha Rama Devi, A. and Prabhakara, K. and Dutta, Usha (2002) Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones. Annales de Génétique, 45 (1). pp. 13-5. ISSN 0003-3995

Radha Rama Devi, A. and Naik, U. and Dutta, Usha and Srikanth, and Prabhakara, K. (2002) De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation. American Journal of Medical Genetics A, 113 (2). pp. 190-192. ISSN 0148-7299

This list was generated on Fri Mar 29 20:22:58 2024 IST.