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Indian Pediatrics
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June 10, 2011
Partial monosomy 7q
Rajitha Ponnala, Ashwin Dalal
Clinical Dysmorphology
|
September 13, 2005
Hemihyperplasia with Ehlers-Danlos syndrome like skin changes
Ashwin Dalal, Shubha R Phadke
Gene
|
September 1, 2015
Whole exome sequencing identifies a novel frameshift mutation in GPC3 gene in a patient with overgrowth syndrome
Aneek Das Bhowmik, Ashwin Dalal
Cytogenetic and Genome Research
|
October 30, 2025
Deciphering the Structural Variants by Long-Read Genome Sequencing: Technology, Applications, and Case Illustrations
Usha R Dutta, Ashwin Dalal
Clinical Dysmorphology
|
December 13, 2006
Short stature, ulnar deviation of hands with absent carpals and joint contractures: a new syndrome
Shubha R Phadke, Ashwin Dalal
European Journal of Medical Genetics
|
December 23, 2015
Renal dysfunction in sibs with band like calcification with simplified gyration and polymicrogyria: Report of a new mutation and review of literature
Shagun Aggarwal, Ashish Bahal, Ashwin Dalal
Journal of Biosciences
|
February 22, 2024
Rare genetic diseases in India: Steps toward a nationwide mission program
Anjana Kar, Sundaravadivel P, Ashwin Dalal
Journal of Reproduction & Infertility
|
June 12, 2014
A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report
Usha R Dutta, Rajitha Ponnala, Ashwin Dalal
Indian Pediatrics
|
February 2, 2022
Indian Undiagnosed Diseases Program (I-UDP) - The Unmet Need
Ratna Dua Puri, Ashwin Dalal, Amita Moirangthem
Indian Pediatrics
|
September 12, 2017
Variable Expressivity and Response to Bisphosphonate Therapy in a Family with Osteoporosis Pseudoglioma Syndrome
Karthik B Tallapaka, Prajnya Ranganath, Ashwin Dalal
Page
of 13
Search research articles
Search
Showing results (1-10 of 123) with videos related to
Sort By:
Page
of 13
Indian Pediatrics
|
June 10, 2011
Partial monosomy 7q
Rajitha Ponnala, Ashwin Dalal
Clinical Dysmorphology
|
September 13, 2005
Hemihyperplasia with Ehlers-Danlos syndrome like skin changes
Ashwin Dalal, Shubha R Phadke
Gene
|
September 1, 2015
Whole exome sequencing identifies a novel frameshift mutation in GPC3 gene in a patient with overgrowth syndrome
Aneek Das Bhowmik, Ashwin Dalal
Cytogenetic and Genome Research
|
October 30, 2025
Deciphering the Structural Variants by Long-Read Genome Sequencing: Technology, Applications, and Case Illustrations
Usha R Dutta, Ashwin Dalal
Clinical Dysmorphology
|
December 13, 2006
Short stature, ulnar deviation of hands with absent carpals and joint contractures: a new syndrome
Shubha R Phadke, Ashwin Dalal
European Journal of Medical Genetics
|
December 23, 2015
Renal dysfunction in sibs with band like calcification with simplified gyration and polymicrogyria: Report of a new mutation and review of literature
Shagun Aggarwal, Ashish Bahal, Ashwin Dalal
Journal of Biosciences
|
February 22, 2024
Rare genetic diseases in India: Steps toward a nationwide mission program
Anjana Kar, Sundaravadivel P, Ashwin Dalal
Journal of Reproduction & Infertility
|
June 12, 2014
A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report
Usha R Dutta, Rajitha Ponnala, Ashwin Dalal
Indian Pediatrics
|
February 2, 2022
Indian Undiagnosed Diseases Program (I-UDP) - The Unmet Need
Ratna Dua Puri, Ashwin Dalal, Amita Moirangthem
Indian Pediatrics
|
September 12, 2017
Variable Expressivity and Response to Bisphosphonate Therapy in a Family with Osteoporosis Pseudoglioma Syndrome
Karthik B Tallapaka, Prajnya Ranganath, Ashwin Dalal
Page
of 13