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American Journal of Medical Genetics. Part A
|
July 18, 2020
Sotos syndrome in two children from India
Inusha Panigrahi, Chakshu Chaudhry
American Journal of Medical Genetics. Part A
|
July 18, 2020
Indian child with novel variant in OFD1 gene
Inusha Panigrahi, Chirag Ahuja, Chakshu Chaudhry
Tropical Doctor
|
May 22, 2020
Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north India
Deepanjan Bhattacharya, Inusha Panigrahi, Chakshu Chaudhry
BMJ Case Reports
|
January 29, 2021
Bardet-Biedl syndrome presenting with laryngeal web and bifid epiglottis
Parminder Kaur, Chakshu Chaudhry, Harsha Neelam, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2020
Wolf-Hirschhorn syndrome: A case series from India
Chakshu Chaudhry, Anit Kaur, Inusha Panigrahi, et al.
BMJ Case Reports
|
January 18, 2023
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the <i>CREBBP</i> gene
Sagarika Snehi, Anupriya Kaur, Chakshu Chaudhry, et al.
Journal of Pediatric Genetics
|
January 1, 2024
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations
Chakshu Chaudhry, Divya Kumari, Inusha Panigrahi, et al.
American Journal of Medical Genetics. Part A
|
February 2, 2021
Ayme gripp syndrome in an Indian patient
Chakshu Chaudhry, Parminder Kaur, Priyanka Srivastava, et al.
Laboratory Medicine
|
November 18, 2021
Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency
Parminder Kaur, Chakshu Chaudhry, Inusha Panigrahi, et al.
Case Reports in Genetics
|
November 15, 2021
Overlapping Phenotypes in Osteopetrosis and Pycnodysostosis in Asian-Indians
Parminder Kaur, Inusha Panigrahi, Harleen Kaur, et al.
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Search research articles
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Showing results (1-10 of 22) with videos related to
Sort By:
Page
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American Journal of Medical Genetics. Part A
|
July 18, 2020
Sotos syndrome in two children from India
Inusha Panigrahi, Chakshu Chaudhry
American Journal of Medical Genetics. Part A
|
July 18, 2020
Indian child with novel variant in OFD1 gene
Inusha Panigrahi, Chirag Ahuja, Chakshu Chaudhry
Tropical Doctor
|
May 22, 2020
Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north India
Deepanjan Bhattacharya, Inusha Panigrahi, Chakshu Chaudhry
BMJ Case Reports
|
January 29, 2021
Bardet-Biedl syndrome presenting with laryngeal web and bifid epiglottis
Parminder Kaur, Chakshu Chaudhry, Harsha Neelam, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2020
Wolf-Hirschhorn syndrome: A case series from India
Chakshu Chaudhry, Anit Kaur, Inusha Panigrahi, et al.
BMJ Case Reports
|
January 18, 2023
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the <i>CREBBP</i> gene
Sagarika Snehi, Anupriya Kaur, Chakshu Chaudhry, et al.
Journal of Pediatric Genetics
|
January 1, 2024
Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations
Chakshu Chaudhry, Divya Kumari, Inusha Panigrahi, et al.
American Journal of Medical Genetics. Part A
|
February 2, 2021
Ayme gripp syndrome in an Indian patient
Chakshu Chaudhry, Parminder Kaur, Priyanka Srivastava, et al.
Laboratory Medicine
|
November 18, 2021
Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency
Parminder Kaur, Chakshu Chaudhry, Inusha Panigrahi, et al.
Case Reports in Genetics
|
November 15, 2021
Overlapping Phenotypes in Osteopetrosis and Pycnodysostosis in Asian-Indians
Parminder Kaur, Inusha Panigrahi, Harleen Kaur, et al.
Page
of 3