Beta Thalassemia and Klinefelter syndrome: a rare occurrence von Billapati, Sushmitha, Sowmya, G. C, Tapadia, R. S, Dutta, Usha R

Volltext

The history of human cytogenetics in India—A review von Dutta, Usha R.

Volltext

A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report von Dutta, Usha R, Ponnala, Rajitha, Dalal, Ashwin

Volltext

Whole exome sequencing identifies a novel 5 Mb deletion at 14q12 region in a patient with global developmental delay, microcephaly and seizures von Vineeth, Venugopal S., Dutta, Usha R., Tallapaka, Karthik, Das Bhowmik, Aneek, Dalal, Ashwin

Volltext

Breakpoint mapping of a novel de novo translocation t(X;20)(q11.1;p13) by positional cloning and long read sequencing von 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

Volltext

Molecular and cytogenetic characterization of two patients with recurrent miscarriages and X-autosome translocation von Dutta, Usha R, Pidugu, Vijaya Kumar, Dalal, Ashwin B

Volltext

Cytogenomic Characterization of a Novel de novo Balanced Reciprocal Translocation t(1;12) by Genome Sequencing Leading to Fusion Gene Formation of EYA3/EFCAB4b von Dutta, Usha R., Bhattacherjee, Amrita, Bahal, Ashish, Posanapally, Laxmi P., Lone, Kaisar A., Bathula, Siddardha, Dalal, Ashwin

Volltext

Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review von Dutta, Usha R., Rajitha, P., Pidugu, Vijaya Kumar, Dalal, Ashwin B.

Volltext

A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: Molecular characterization of the marker von Dutta, Usha R., Vempally, Subhash, Ranganath, Prajnya, Dalal, Ashwin

Volltext

Cytogenetic and molecular study of 370 infertile men in South India highlighting the importance of copy number variations by multiplex ligation‐dependent probe amplification von Dutta, Usha R., Suttur, Malini S., Venugopal, Vineeth S., Posanapally, Laxmi Priyanka, Gopalasetty, Sravani, Talwar, Sangamesh, Anand, Suhana, Billapati, Sushmita, Jesudasan, Rachel A., Dalal, Ashwin

Volltext

Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature von Dutta, Usha R, Hansmann, Ingo, Schlote, Dietmar

Volltext

Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS von Dutta, Usha R, Swamy, Venugopala, Ponnala, Rajitha, Aggarwal, Shagun, Dalal, Ashwin

Volltext

Molecular Cytogenetic Characterization of a Non-Robertsonian Dicentric Chromosome 14;19 Identified in a Girl with Short Stature and Amenorrhea von Dutta, Usha R., Pidugu, Vijaya Kumar, Dalal, Ashwin

Volltext

Mosaic Down syndrome with a marker: Molecular cytogenetic characterization of the marker chromosome von Dutta, Usha R., Pidugu, Vijaya Kumar, Goud, Venkatesh, Dalal, Ashwin B.

Volltext

High incidence of sperm dysfunction in a varicocele infertile man: case report von Vineeth, VS, Malini, Suttur S, Sreenivasa, G, Dutta, Usha R

Volltext

Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development von Dutta, Usha R., Pidugu, Vijaya Kumar, Goud, Ch. Venkateshwar, Hoefers, Christiane, Hagemann, Monika, Dalal, Ashwin

Volltext

ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation von 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

Volltext

Chromosomal Abnormalities in Amenorrhea: A Retrospective Study and Review of 637 Patients in South India von Dutta, Usha R, Ponnala, Rajitha, Pidugu, Vijaya Kumar, Dalal, Ashwin B

Volltext

Precision in chromosome identification with leads in molecular cytogenetics: An illustrated review von Dutta, Usha R.

Volltext

A novel mosaic complex supernumerary marker chromosome in a girl with seizures: systematic characterization of the complex marker von Dutta, Usha R., Bahal, Ashish, Vineeth, V.S., Sarvade, Vasantha, Ranganath, Prajnya, Dalal, Ashwin

Volltext