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Indian Journal of Pediatrics
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October 7, 2023
Next-Generation Sequencing in Unexplained Intellectual Disability
Sapna Sandal, Ishwar Chander Verma, Sunita Bijarnia Mahay, et al.
Journal of Human Genetics
|
March 31, 2025
A novel case of autosomal-dominant cutis laxa caused by a de novo likely pathogenic variant in ALDH18A1: case report and literature review
Firoz Ahmad, Pradnya Gadgil, Noopur Navandar, et al.
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Showing results (11-20 of 12) with videos related to
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This site can display upto 12 results.
Indian Journal of Pediatrics
|
October 7, 2023
Next-Generation Sequencing in Unexplained Intellectual Disability
Sapna Sandal, Ishwar Chander Verma, Sunita Bijarnia Mahay, et al.
Journal of Human Genetics
|
March 31, 2025
A novel case of autosomal-dominant cutis laxa caused by a de novo likely pathogenic variant in ALDH18A1: case report and literature review
Firoz Ahmad, Pradnya Gadgil, Noopur Navandar, et al.
Page
of 2