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Case Reports in Genetics|August 4, 2025
Chromosome 1p31.1 Deletion: A Case With Developmental Delay, Hypotonia, Cryptorchidism, Abnormal Oral Frenulum, and Feet DeformityTatiana Mikhailova, Ria GargBMJ Case Reports|February 25, 2026
Orofacial clefting in <i>PHF6</i>-related Börjeson-Forssman-Lehmann syndromeDibyendu Dutta, Ria GargGenes|February 27, 2026
Xp22.33 Duplication Encompassing PAR1 in a Male with Syndromic Neurodevelopmental Disorder and Tall StatureDibyendu Dutta, Xi Luo, Ria GargCurrent Cardiology Reports|October 8, 2021
Established and Emerging Techniques for Pericardial Imaging with Cardiac Magnetic ResonanceRia Garg, Ezequiel Guzzetti, Michael ChetritBMJ Case Reports|November 6, 2025
<i>ZFHX3</i>-associated neural tube defectDibyendu Dutta, Erfan Aref-Eshghi, Ria GargBMJ Case Reports|July 27, 2025
Rapid genetic testing in the PICU: uncovering COL4A2-related GOULD syndrome in super-refractory status epilepticusKyle Chandler Sporn, Ria Garg, Ai SakonjuJMIR Cancer|December 2, 2020
Information Needs About Cancer Treatment, Fertility, and Pregnancy: Qualitative Descriptive Study of Reddit ThreadsRia Garg, Nevena Rebić, Mary A De VeraIndian Heart Journal|October 25, 2016
Long-term results of percutaneous balloon valvuloplasty of congenital aortic stenosis in adolescents and young adultsNeeraj Awasthy, Ria Garg, S Radhakrishnan, et al.Journal of Cannabis Research|September 9, 2022
The association between cannabis and codeine use: a nationally representative cross-sectional study in CanadaRia Garg, Kam Shojania, Mary A De VeraFrontiers in Pediatrics|April 25, 2025
Case Report: A novel missense variant in <i>ZC4H2</i>, c.196C>T p.(Leu66Phe), is associated with a mild, ZC4H2-related X-linked syndromic intellectual disability (ZARD) phenotypeRia Garg, Wenying Zhang, Julianne E Hartmann, et al.Pageof 5