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Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 23, 2009
Zolendronate in osteogenesis imperfecta
Inusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Clinical Dysmorphology
|
October 29, 2002
Mental retardation, ptosis and polydactyly: a new autosomal recessive syndrome?
Inusha Panigrahi, Shubha R Phadke, S S Agarwal
Annals of Hematology
|
August 6, 2009
Long-term response to deferiprone therapy in Asian Indians
Inusha Panigrahi, Ram K Marwaha, Rashmi R Das
Molecular Biology Reports
|
May 18, 2011
STR markers for detecting heterogeneity in Indian population
Shalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatric Neurology
|
March 25, 2015
Seizure as the presenting manifestation in Griscelli syndrome type 2
Inusha Panigrahi, Renu Suthar, Amit Rawat, 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.
Journal of Pediatric Genetics
|
January 23, 2023
Genetic Defects in Children with Cardiac Anomalies/Malformations: Noonan and CFC Syndromes
Divya Kumari, Deepti Chaudhary, Inusha Panigrahi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
July 16, 2021
Study of Prothrombotic Gene Variations Associated with the Risk of Development of Thrombosis in Patients with Down Syndrome
Chandreswara Raju Kataru, Vinodhini Krishnakumar, Inusha Panigrahi, et al.
Indian Journal of Human Genetics
|
November 20, 2012
Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
Suresh Kumar, Renu Suthar, Inusha Panigrahi, et al.
BMJ Case Reports
|
April 22, 2019
Hunter syndrome with persistent thrombocytopenia
Inusha Panigrahi, Manoj Dhanorkar, Siyaram Didel, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 158) with videos related to
Sort By:
Page
of 16
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 23, 2009
Zolendronate in osteogenesis imperfecta
Inusha Panigrahi, Rashmi Ranjan Das, Ram Kumar Marwaha
Clinical Dysmorphology
|
October 29, 2002
Mental retardation, ptosis and polydactyly: a new autosomal recessive syndrome?
Inusha Panigrahi, Shubha R Phadke, S S Agarwal
Annals of Hematology
|
August 6, 2009
Long-term response to deferiprone therapy in Asian Indians
Inusha Panigrahi, Ram K Marwaha, Rashmi R Das
Molecular Biology Reports
|
May 18, 2011
STR markers for detecting heterogeneity in Indian population
Shalu Jain, Inusha Panigrahi, Jayesh Sheth, et al.
Pediatric Neurology
|
March 25, 2015
Seizure as the presenting manifestation in Griscelli syndrome type 2
Inusha Panigrahi, Renu Suthar, Amit Rawat, 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.
Journal of Pediatric Genetics
|
January 23, 2023
Genetic Defects in Children with Cardiac Anomalies/Malformations: Noonan and CFC Syndromes
Divya Kumari, Deepti Chaudhary, Inusha Panigrahi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
July 16, 2021
Study of Prothrombotic Gene Variations Associated with the Risk of Development of Thrombosis in Patients with Down Syndrome
Chandreswara Raju Kataru, Vinodhini Krishnakumar, Inusha Panigrahi, et al.
Indian Journal of Human Genetics
|
November 20, 2012
Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
Suresh Kumar, Renu Suthar, Inusha Panigrahi, et al.
BMJ Case Reports
|
April 22, 2019
Hunter syndrome with persistent thrombocytopenia
Inusha Panigrahi, Manoj Dhanorkar, Siyaram Didel, et al.
Page
of 16