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Ratna Puri

Showing results (1-10 of 22) with videos related to

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Journal of Clinical Ultrasound : JCU|April 6, 2007
Severe form of congenital cerebral and cerebellar atrophy: a neurodegenerative disorder of fetal onsetShubha Phadke, Ratna Puri, Rajendra Phadke
Indian Journal of Pediatrics|January 5, 2005
Gerodermia OsteodysplasticaRitu Paul, Seema Kapoor, Ratna Puri, et al.
Indian Journal of Human Genetics|November 20, 2012
A familial deletion 4q syndrome: An outcome of a paracentric inversionMeena Lall, Ratna Puri, Pushpa Saviour, et al.
BMJ Case Reports|October 11, 2020
Novel homozygous missense mutation in ABCA3 protein leading to severe respiratory distress in term infantNaveen Parkash Gupta, Anil Batra, Ratna Puri, et al.
Indian Journal of Orthopaedics|October 20, 2009
Molecular studies of achondroplasiaRisha Nahar, Renu Saxena, Sudha Kohli, et al.
Materials (Basel, Switzerland)|July 30, 2025
Synergistic Effect of Calcination Temperature and Silver Doping on Photocatalytic Performance of ZnO MaterialK Kusdianto, Nurdiana Ratna Puri, Manabu Shimada, et al.
Molecular Cytogenetics|September 23, 2011
A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosumMeena Lall, Seema Thakur, Ratna Puri, et al.
Genetic Testing and Molecular Biomarkers|February 4, 2012
Mutation analysis of the CFTR gene in 225 children: identification of five novel severe and seven reported severe mutationsKabir Sachdeva, Renu Saxena, Ratna Puri, et al.
Molecules (Basel, Switzerland)|August 28, 2025
Comparative Study of ZnO and ZnO-Ag Particle Synthesis via Flame and Spray Pyrolysis for the Degradation of Methylene BlueKusdianto, Nurdiana Ratna Puri, Adhi Setiawan, et al.
BMC Medical Genetics|October 5, 2018
Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in IndiaJayesh Sheth, Dhairya Pancholi, Mehul Mistri, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Clinical Ultrasound : JCU|April 6, 2007
Severe form of congenital cerebral and cerebellar atrophy: a neurodegenerative disorder of fetal onsetShubha Phadke, Ratna Puri, Rajendra Phadke
Indian Journal of Pediatrics|January 5, 2005
Gerodermia OsteodysplasticaRitu Paul, Seema Kapoor, Ratna Puri, et al.
Indian Journal of Human Genetics|November 20, 2012
A familial deletion 4q syndrome: An outcome of a paracentric inversionMeena Lall, Ratna Puri, Pushpa Saviour, et al.
BMJ Case Reports|October 11, 2020
Novel homozygous missense mutation in ABCA3 protein leading to severe respiratory distress in term infantNaveen Parkash Gupta, Anil Batra, Ratna Puri, et al.
Indian Journal of Orthopaedics|October 20, 2009
Molecular studies of achondroplasiaRisha Nahar, Renu Saxena, Sudha Kohli, et al.
Materials (Basel, Switzerland)|July 30, 2025
Synergistic Effect of Calcination Temperature and Silver Doping on Photocatalytic Performance of ZnO MaterialK Kusdianto, Nurdiana Ratna Puri, Manabu Shimada, et al.
Molecular Cytogenetics|September 23, 2011
A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosumMeena Lall, Seema Thakur, Ratna Puri, et al.
Genetic Testing and Molecular Biomarkers|February 4, 2012
Mutation analysis of the CFTR gene in 225 children: identification of five novel severe and seven reported severe mutationsKabir Sachdeva, Renu Saxena, Ratna Puri, et al.
Molecules (Basel, Switzerland)|August 28, 2025
Comparative Study of ZnO and ZnO-Ag Particle Synthesis via Flame and Spray Pyrolysis for the Degradation of Methylene BlueKusdianto, Nurdiana Ratna Puri, Adhi Setiawan, et al.
BMC Medical Genetics|October 5, 2018
Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in IndiaJayesh Sheth, Dhairya Pancholi, Mehul Mistri, et al.
Pageof 3