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R Phadke

Showing results (91-100 of 311) with videos related to

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Neurology India|April 8, 2004
Molecular diagnosis and genetic counseling for fragile X mental retardationU B Pandey, S R Phadke, B Mittal
Journal of Medical Genetics|December 10, 1997
Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?R Gulati, S R Phadke, S S Agarwal
Clinical Dysmorphology|August 7, 2018
Extending the phenotype and an ECEL1 gene mutation in distal arthrogryposis type 5DArchana Rai, Ratna D Puri, Shubha R Phadke
Hematology (Amsterdam, Netherlands)|July 12, 2008
Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia majorHimanshu Goel, K M Girisha, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 12, 2002
Recurrence of complex camptopolydactyly in a sibling suggestive of autosomal recessive mode of inheritanceShubha R Phadke, Savita Agarwal, Ratna Dua Puri
Neurology India|February 7, 2001
Retrocerebellar arachnoid cyst with syringomyelia: a case reportR Jain, V Sawlani, R Phadke, et al.
Indian Pediatrics|June 1, 1994
Post mortem radiography of perinatal deaths: an aid to genetic counsellingA K Sharma, A Haldar, S R Phadke
Indian Pediatrics|August 26, 1998
Acromesomelic dwarfism: report of a family with two affected siblingsS Danda, S R Phadke, S S Agarwal
The Indian Journal of Medical Research|September 20, 2022
Haemophilia management programme: Transformation during COVID-19Haseena Sait, Shruti M Sajjan, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 15, 2018
Malan syndrome: Extension of genotype and phenotype spectrumArchana Rai, Dhanya Lakshmi Narayanan, Shubha R Phadke
Pageof 32

Showing results (91-100 of 311) with videos related to

Sort By:
Pageof 32
Neurology India|April 8, 2004
Molecular diagnosis and genetic counseling for fragile X mental retardationU B Pandey, S R Phadke, B Mittal
Journal of Medical Genetics|December 10, 1997
Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?R Gulati, S R Phadke, S S Agarwal
Clinical Dysmorphology|August 7, 2018
Extending the phenotype and an ECEL1 gene mutation in distal arthrogryposis type 5DArchana Rai, Ratna D Puri, Shubha R Phadke
Hematology (Amsterdam, Netherlands)|July 12, 2008
Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia majorHimanshu Goel, K M Girisha, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 12, 2002
Recurrence of complex camptopolydactyly in a sibling suggestive of autosomal recessive mode of inheritanceShubha R Phadke, Savita Agarwal, Ratna Dua Puri
Neurology India|February 7, 2001
Retrocerebellar arachnoid cyst with syringomyelia: a case reportR Jain, V Sawlani, R Phadke, et al.
Indian Pediatrics|June 1, 1994
Post mortem radiography of perinatal deaths: an aid to genetic counsellingA K Sharma, A Haldar, S R Phadke
Indian Pediatrics|August 26, 1998
Acromesomelic dwarfism: report of a family with two affected siblingsS Danda, S R Phadke, S S Agarwal
The Indian Journal of Medical Research|September 20, 2022
Haemophilia management programme: Transformation during COVID-19Haseena Sait, Shruti M Sajjan, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 15, 2018
Malan syndrome: Extension of genotype and phenotype spectrumArchana Rai, Dhanya Lakshmi Narayanan, Shubha R Phadke
Pageof 32