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Wendy Chung

Showing results (31-40 of 92) with videos related to

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The Hastings Center Report|January 21, 2015
The authors replyPaul S Appelbaum, Wendy Chung, Abby J Fyer, et al.
Diagnostic Microbiology and Infectious Disease|December 10, 2013
Clinical features of West Nile virus epidemic in Dallas, Texas, 2012Lori Racsa, Rita Gander, Wendy Chung, et al.
Plos One|December 7, 2007
A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic responseJohn R Bankston, Minerva Yue, Wendy Chung, et al.
Biorxiv : the Preprint Server for Biology|February 24, 2025
MYRF is Essential in Mesothelial Cells to Promote Lung Development and MaturationGidsela Luna, Jamie Verheyden, Chunting Tan, et al.
Clinical Genetics|March 30, 2026
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental AbnormalitiesEugénie Koumakis, Céline Huber, Wendy Chung, et al.
Journal of Medical Genetics|August 27, 2020
A novel homozygous variant in <i>TRAPPC2L</i> results in a neurodevelopmental disorder and disrupts TRAPP complex functionNoraldin Al-Deri, Volkan Okur, Priyanka Ahimaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2021
Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Catherine Rehder, Lora J H Bean, David Bick, et al.
Blood|November 16, 2006
Gene expression patterns in blood leukocytes discriminate patients with acute infectionsOctavio Ramilo, Windy Allman, Wendy Chung, et al.
Frontiers in Pediatrics|July 26, 2021
Case Report: Esophageal Bronchus in a Neonate, With Image, Histological, and Molecular AnalysisStephen L Trisno, Nara S Higano, Dan Kechele, et al.
Journal of Medical Genetics|October 10, 2022
Clinical, neuroimaging and molecular characteristics of <i>PPP2R5D</i>-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype-phenotype analysisNora Oyama, Pieter Vaneynde, Sara Reynhout, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
The Hastings Center Report|January 21, 2015
The authors replyPaul S Appelbaum, Wendy Chung, Abby J Fyer, et al.
Diagnostic Microbiology and Infectious Disease|December 10, 2013
Clinical features of West Nile virus epidemic in Dallas, Texas, 2012Lori Racsa, Rita Gander, Wendy Chung, et al.
Plos One|December 7, 2007
A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic responseJohn R Bankston, Minerva Yue, Wendy Chung, et al.
Biorxiv : the Preprint Server for Biology|February 24, 2025
MYRF is Essential in Mesothelial Cells to Promote Lung Development and MaturationGidsela Luna, Jamie Verheyden, Chunting Tan, et al.
Clinical Genetics|March 30, 2026
Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental AbnormalitiesEugénie Koumakis, Céline Huber, Wendy Chung, et al.
Journal of Medical Genetics|August 27, 2020
A novel homozygous variant in <i>TRAPPC2L</i> results in a neurodevelopmental disorder and disrupts TRAPP complex functionNoraldin Al-Deri, Volkan Okur, Priyanka Ahimaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2021
Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Catherine Rehder, Lora J H Bean, David Bick, et al.
Blood|November 16, 2006
Gene expression patterns in blood leukocytes discriminate patients with acute infectionsOctavio Ramilo, Windy Allman, Wendy Chung, et al.
Frontiers in Pediatrics|July 26, 2021
Case Report: Esophageal Bronchus in a Neonate, With Image, Histological, and Molecular AnalysisStephen L Trisno, Nara S Higano, Dan Kechele, et al.
Journal of Medical Genetics|October 10, 2022
Clinical, neuroimaging and molecular characteristics of <i>PPP2R5D</i>-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype-phenotype analysisNora Oyama, Pieter Vaneynde, Sara Reynhout, et al.
Pageof 10