Ngā hua rapu - Jayesh Sheth
- E whakaatu ana i te 1 - 5 hua o te 5
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Burden of Lysosomal Storage Disorders in India: Experience of 387 Affected Children from a Single Diagnostic Facility mā Jayesh Sheth, Mehul Mistri, Frenny Sheth, Raju Shah, Ashish Bavdekar, Koumudi Godbole, Nidhish Nanavaty, Chaitanya Datar, Mahesh Kamate, Nrupesh Oza, Chitra Ankleshwaria, Sanjeev Mehta, Marie Jackson
I whakaputaina 2013Artigo -
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Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test mā Frenny Sheth, Jhanvi Shah, Deepika Jain, Siddharth Shah, Harsh Patel, Ketan J. Patel, Dhaval Solanki, Anand Iyer, Bhargavi Menghani, Priti Mhatre, Sanjiv Mehta, Shruti Bajaj, Vishal Patel, Manoj Pandya, Deepak Dhami, Darshan Patel, Jayesh Sheth, Harsh Sheth
I whakaputaina 2023Artigo -
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Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation mā Jayesh Sheth, Riddhi Bhavsar, Mehul Mistri, Dhairya Pancholi, Ashish Bavdekar, Ashwin Dalal, Prajnya Ranganath, Katta M. Girisha, Anju Shukla, Shubha R. Phadke, Ratna Dua Puri, Inusha Panigrahi, Anupriya Kaur, Mamta Muranjan, Manisha Goyal, Radha Ramadevi, Raju Shah, Sheela Nampoothiri, Sumita Danda, Chaitanya Datar, Seema Kapoor, Seema S. Bhatwadekar, Frenny Sheth
I whakaputaina 2019Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Medicine
Internal medicine
Biology
Diabetes mellitus
Disease
Endocrinology
Gene
Genetics
Hemoglobin
Human genetics
Mutation
Pathology
Type 2 diabetes
Association (psychology)
Autism
Autism spectrum disorder
Candidate gene
Cell cycle
Chromosome
Concordance
Copy-number variation
Cytogenetics
DNA sequencing
Dyslipidemia
Enzyme replacement therapy
Exome sequencing
Fabry disease
Gangliosidosis
Genetic architecture
Genetic testing