Molecular and cytogenetic characterization of two patients with recurrent miscarriages and X-autosome translocation

Por Dutta, Usha R., Pidugu, Vijaya Kumar, Dalal, Ashwin B.
Publicado em 2012

Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy- coxa vara- pericarditis (CACP) syndrome

Por Nandagopalan, Rajashree S., Phadke, Shubha R., Dalal, Ashwin B., Ranganath, Prajnya
Publicado em 2014

Brothers with constrictive pericarditis – A novel mutation in a rare disease

Por Patil, Devendra V., Phadke, Milind S., Pahwa, Jivtesh S., Dalal, Ashwin B.
Publicado no Indian Heart J (2016)

Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review

Por Dutta, Usha R., Rajitha, P., Pidugu, Vijaya Kumar, Dalal, Ashwin B.
Publicado em 2010

Novel mutations in the neuraminidase-1 (NEU1) gene in two patients of sialidosis in India

Por Ranganath, Prajnya, Sharma, Vishakha, Danda, Sumita, Nandineni, Madhusudan R., Dalal, Ashwin B.
Publicado em 2012

A Balanced Reciprocal Translocation T (X;20) in A Girl with Seizures and Intellectual Disability Disrupting ARHGEF9

Por Dutta, Usha R, Pidugu, Vijaya Kumar, Kalscheuer, Vera M, Dalal, Ashwin B
Publicado em 2014

Molecular analysis of mucopolysaccharidoses: identification and characterization of pathogenic mutations in Indian population

Por Uttarilli, Anusha, Jain, S Jamal Md Nurul, Dalal, Ashwin B, Ranganath, Prajnya, Phadke, Shubha R, Kumar, Girisha, Sankar, Patil, SJ, Kabra, Madhulika, Danda, Sumita
Publicado em 2014

Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI

Por Uttarilli, Anusha, Ranganath, Prajnya, Jain, S. Jamal Md Nurul, Krishna, Prasad C., Sinha, Anupam, Verma, Ishwar C., Phadke, Shubha R., Puri, Ratna D., Danda, Sumita, Muranjan, Mamta N., Jevalikar, Ganesh, Nagarajaram, H. A., Dalal, Ashwin B.
Publicado no Indian J Med Res (2015)