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R Phadke

Showing results (61-70 of 311) with videos related to

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Clinical Dysmorphology|October 18, 2003
Catel-Manzke syndrome without cleft palate: a case reportRatna Dua Puri, Shubha R Phadke
American Journal of Medical Genetics. Part A|May 26, 2017
A novel variant in MED12 gene: Further delineation of phenotypeDhanya L Narayanan, Shubha R Phadke
Neuropathology and Applied Neurobiology|August 28, 2016
Metastatic renal cell carcinoma metastasising into a cerebral cavernous malformationJ Shapey, R Phadke, N Kitchen
Indian Journal of Pediatrics|January 5, 2007
Asphyxiating thoracic dystrophy with facial dysmorphismV H Sankar, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 14, 2006
Pericentric inversion causing duplication and deletion of chromosome region 13q22 --> qter in the offspringSiddramappa J Patil, Shubha R Phadke
Journal of Genetics|June 3, 2020
Hypotonic infant with Pallister-Killian syndrome diagnosed by cytogenetic microarray, without pigmentary skin changes and malformationsAnup Rawool, Priyanka Srivastava, Shubha R Phadke
Clinical Dysmorphology|May 31, 2018
A large interstitial 11q deletion with isolated mild intellectual disability: review of the literature for genotype-phenotype correlationMeenakshi Lallar, Priyanka Srivastava, Shubha R Phadke
Neurology India|September 8, 2017
Hyperekplexia: A forgotten diagnosis clinched by next-generation sequencingMeenakshi Lallar, Anukool Srivastava, Shubha R Phadke
Journal of Clinical Laboratory Analysis|December 30, 2014
A Mutagenic Primer Assay for Genotyping of the CRHR1 Gene Rare Variant rs1876828 (A/G) in Asians: A Cost-Effective SNP TypingNeeraj Sharma, Shally Awasthi, Shubha R Phadke
Indian Journal of Pediatrics|September 29, 2006
Unbalanced X; autosome translocationNeerja Gupta, Himanshu Goel, Shubha R Phadke
Pageof 32

Showing results (61-70 of 311) with videos related to

Sort By:
Pageof 32
Clinical Dysmorphology|October 18, 2003
Catel-Manzke syndrome without cleft palate: a case reportRatna Dua Puri, Shubha R Phadke
American Journal of Medical Genetics. Part A|May 26, 2017
A novel variant in MED12 gene: Further delineation of phenotypeDhanya L Narayanan, Shubha R Phadke
Neuropathology and Applied Neurobiology|August 28, 2016
Metastatic renal cell carcinoma metastasising into a cerebral cavernous malformationJ Shapey, R Phadke, N Kitchen
Indian Journal of Pediatrics|January 5, 2007
Asphyxiating thoracic dystrophy with facial dysmorphismV H Sankar, Shubha R Phadke
American Journal of Medical Genetics. Part A|December 14, 2006
Pericentric inversion causing duplication and deletion of chromosome region 13q22 --> qter in the offspringSiddramappa J Patil, Shubha R Phadke
Journal of Genetics|June 3, 2020
Hypotonic infant with Pallister-Killian syndrome diagnosed by cytogenetic microarray, without pigmentary skin changes and malformationsAnup Rawool, Priyanka Srivastava, Shubha R Phadke
Clinical Dysmorphology|May 31, 2018
A large interstitial 11q deletion with isolated mild intellectual disability: review of the literature for genotype-phenotype correlationMeenakshi Lallar, Priyanka Srivastava, Shubha R Phadke
Neurology India|September 8, 2017
Hyperekplexia: A forgotten diagnosis clinched by next-generation sequencingMeenakshi Lallar, Anukool Srivastava, Shubha R Phadke
Journal of Clinical Laboratory Analysis|December 30, 2014
A Mutagenic Primer Assay for Genotyping of the CRHR1 Gene Rare Variant rs1876828 (A/G) in Asians: A Cost-Effective SNP TypingNeeraj Sharma, Shally Awasthi, Shubha R Phadke
Indian Journal of Pediatrics|September 29, 2006
Unbalanced X; autosome translocationNeerja Gupta, Himanshu Goel, Shubha R Phadke
Pageof 32