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Journal of Pediatric Genetics
|
February 8, 2021
Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss
Meenakshi Lallar, Veronica Arora, Renu Saxena, et al.
Journal of Pediatric Genetics
|
November 6, 2024
<i>CDKN1C</i> -Related Beckwith-Wiedemann Syndrome: First Patient from India
Veronica Arora, Aashita Takkar, Sudhisha Dubey, et al.
Journal of Pediatric Genetics
|
December 1, 2021
Implications of a Genetic Etiology for Renal Transplant: Early-Onset Alport Syndrome with a Novel Mutation
Ravi Kumar Singh, Veronica Arora, Vaibhav Tiwari, et al.
Journal of Clinical Imaging Science
|
June 8, 2022
Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up
Aakriti Kapoor, Tushar Kapoor, Aakaar Kapoor, et al.
Indian Journal of Pediatrics
|
June 24, 2026
Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing
Prajnya Ranganath, Sankar Vh, Kausik Mandal, et al.
Autopsy & Case Reports
|
October 24, 2019
Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation
Veronica Arora, Sunita Bijarnia-Mahay, Samarth Kulshreshtra, et al.
Journal of Clinical and Experimental Hepatology
|
March 11, 2015
Hepatitis B Virus Infection can Cause Hepatocellular Carcinoma in Less Advanced Liver Cirrhosis: A Comparative Study of 142 Patients from North India
Anil Arora, Praveen Sharma, Pankaj Tyagi, et al.
Journal of Medical Case Reports
|
February 28, 2014
Iatrogenic hypervitaminosis D as an unusual cause of persistent vomiting: a case report
Rinkesh Kumar Bansal, Pankaj Tyagi, Praveen Sharma, et al.
Molecular Syndromology
|
February 26, 2019
Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome
Veronica Arora, Shruti Aggarwal, Sunita Bijarnia, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2023
The molecular landscape of oculocutaneous albinism in India and its therapeutic implications
Sudha Kohli, Renu Saxena, Ratna Dua Puri, et al.
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of 4
Search research articles
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Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Journal of Pediatric Genetics
|
February 8, 2021
Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss
Meenakshi Lallar, Veronica Arora, Renu Saxena, et al.
Journal of Pediatric Genetics
|
November 6, 2024
<i>CDKN1C</i> -Related Beckwith-Wiedemann Syndrome: First Patient from India
Veronica Arora, Aashita Takkar, Sudhisha Dubey, et al.
Journal of Pediatric Genetics
|
December 1, 2021
Implications of a Genetic Etiology for Renal Transplant: Early-Onset Alport Syndrome with a Novel Mutation
Ravi Kumar Singh, Veronica Arora, Vaibhav Tiwari, et al.
Journal of Clinical Imaging Science
|
June 8, 2022
Isolated congenital absence of bilateral femur: A rare case report with antenatal diagnosis and postnatal follow-up
Aakriti Kapoor, Tushar Kapoor, Aakaar Kapoor, et al.
Indian Journal of Pediatrics
|
June 24, 2026
Position Statement of the Indian Academy of Medical Genetics on Cytogenetic and Molecular Cytogenetic Testing
Prajnya Ranganath, Sankar Vh, Kausik Mandal, et al.
Autopsy & Case Reports
|
October 24, 2019
Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation
Veronica Arora, Sunita Bijarnia-Mahay, Samarth Kulshreshtra, et al.
Journal of Clinical and Experimental Hepatology
|
March 11, 2015
Hepatitis B Virus Infection can Cause Hepatocellular Carcinoma in Less Advanced Liver Cirrhosis: A Comparative Study of 142 Patients from North India
Anil Arora, Praveen Sharma, Pankaj Tyagi, et al.
Journal of Medical Case Reports
|
February 28, 2014
Iatrogenic hypervitaminosis D as an unusual cause of persistent vomiting: a case report
Rinkesh Kumar Bansal, Pankaj Tyagi, Praveen Sharma, et al.
Molecular Syndromology
|
February 26, 2019
Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome
Veronica Arora, Shruti Aggarwal, Sunita Bijarnia, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2023
The molecular landscape of oculocutaneous albinism in India and its therapeutic implications
Sudha Kohli, Renu Saxena, Ratna Dua Puri, et al.
Page
of 4