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Dhanya Yesodharan

Showing results (1-10 of 31) with videos related to

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Indian Journal of Pediatrics|November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counselingDhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Journal of Pediatric Genetics|November 18, 2017
Osteoglophonic Dysplasia: Phenotypic and Radiological CluesShwetha Kuthiroly, Dhanya Yesodharan, Aneesh Ghosh, et al.
Journal of Human Genetics|July 10, 2019
Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndromeAntonia Howaldt, Sheela Nampoothiri, Dhanya Yesodharan, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 24, 2012
Sirenomelia: case reports and current concepts of pathogenesisMinnie Pillay, Dhanya Yesodharan, Dhanya Lakshmi Narayanan, et al.
Indian Journal of Pediatrics|February 1, 2018
Goltz-Gorlin Syndrome: Revisiting the Clinical SpectrumDhanya Yesodharan, Uta Meyer Zum Büschenfelde, Kerstin Kutsche, et al.
American Journal of Medical Genetics. Part A|November 12, 2020
Lethal Cenani Lenz syndrome in two consecutive pregnancies: Further extension of phenotype from MaldivesDhanya Yesodharan, Vivek Krishnan, Indu R Nair, et al.
Journal of Pediatric Genetics|November 17, 2017
Plexiform Neurofibroma of ClitorisDhanya Yesodharan, Bindu Sudarsanan, Annie Jojo, et al.
Hormones (Athens, Greece)|March 23, 2023
Cost-effective genotyping for classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) in resource-poor settings: multiplex ligation probe amplification (MLPA) with/without sequential next-generation sequencing (NGS)Ana Monteiro, Praveen V Pavithran, Manuprasad Puthukulangara, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11Frederike L Harms, Sheela Nampoothiri, Shams Anazi, et al.
Laboratory Medicine|April 13, 2016
Reciprocal Microduplication of the Williams-Beuren Syndrome Chromosome Region in a 9-Year-Old Omani BoyShruthi Mohan, Sheela Nampoothiri, Dhanya Yesodharan, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Indian Journal of Pediatrics|November 30, 2013
Recurrence of Angelman syndrome in siblings: challenges in genetic counselingDhanya Yesodharan, M V Thampi, Teena Koshy, et al.
Journal of Pediatric Genetics|November 18, 2017
Osteoglophonic Dysplasia: Phenotypic and Radiological CluesShwetha Kuthiroly, Dhanya Yesodharan, Aneesh Ghosh, et al.
Journal of Human Genetics|July 10, 2019
Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndromeAntonia Howaldt, Sheela Nampoothiri, Dhanya Yesodharan, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 24, 2012
Sirenomelia: case reports and current concepts of pathogenesisMinnie Pillay, Dhanya Yesodharan, Dhanya Lakshmi Narayanan, et al.
Indian Journal of Pediatrics|February 1, 2018
Goltz-Gorlin Syndrome: Revisiting the Clinical SpectrumDhanya Yesodharan, Uta Meyer Zum Büschenfelde, Kerstin Kutsche, et al.
American Journal of Medical Genetics. Part A|November 12, 2020
Lethal Cenani Lenz syndrome in two consecutive pregnancies: Further extension of phenotype from MaldivesDhanya Yesodharan, Vivek Krishnan, Indu R Nair, et al.
Journal of Pediatric Genetics|November 17, 2017
Plexiform Neurofibroma of ClitorisDhanya Yesodharan, Bindu Sudarsanan, Annie Jojo, et al.
Hormones (Athens, Greece)|March 23, 2023
Cost-effective genotyping for classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) in resource-poor settings: multiplex ligation probe amplification (MLPA) with/without sequential next-generation sequencing (NGS)Ana Monteiro, Praveen V Pavithran, Manuprasad Puthukulangara, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11Frederike L Harms, Sheela Nampoothiri, Shams Anazi, et al.
Laboratory Medicine|April 13, 2016
Reciprocal Microduplication of the Williams-Beuren Syndrome Chromosome Region in a 9-Year-Old Omani BoyShruthi Mohan, Sheela Nampoothiri, Dhanya Yesodharan, et al.
Pageof 4