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The Journal of Pediatrics|January 16, 2023
Novel Approach to Improve the Identification of the Bleeding Phenotype in Noonan Syndrome and Related RASopathiesLeah Bruno, Jerica Lenberg, Dzung Le, et al.
The Journal of Clinical Investigation|May 15, 2020
Maternal diesel particle exposure promotes offspring asthma through NK cell-derived granzyme BQian Qian, Bidisha Paul Chowdhury, Zehua Sun, et al.
American Journal of Medical Genetics. Part A|November 26, 2025
Expanding the Phenotype of Syndromic SLC30A9-Associated DiseaseNaomi E Wagner, Shadi M AlAshwal, Jerica Lenberg, et al.
Virus Research|October 21, 2017
Brief introduction of current technologies in isolation of broadly neutralizing HIV-1 antibodiesZehua Sun, Lixin Yan, Jiansong Tang, et al.
American Journal of Medical Genetics. Part A|January 31, 2023
Further delineation of the CWC27-associated spliceosomeopathy: Case report and review of the literatureShaden H Yassin, Riley Henderson, Jerica Lenberg, et al.
Cold Spring Harbor Molecular Case Studies|June 12, 2021
Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiencyMallory J Owen, Jerica Lenberg, Annette Feigenbaum, et al.
Cold Spring Harbor Molecular Case Studies|April 22, 2021
Expanding the genotypic spectrum of <i>ACTG2</i>-related visceral myopathyKiely N James, Megan Lau, Katayoon Shayan, et al.
Clinical Genetics|October 5, 2024
Consolidating the Role of Mutated ATP2B2 in Neurodevelopmental and Cerebellar PathologiesAntonia M Stehr, Jerica Lenberg, Jennifer Friedman, et al.
HGG Advances|October 27, 2025
Splicing and frameshift variants in QSER1 may be involved in developmental phenotypesMegan C Fischer, Linda M Reis, Jerica Lenberg, et al.
Pediatric Neurology|October 18, 2024
The Face and Features of RNU4-2: A New, Common, Recognizable, Yet Hidden Neurodevelopmental DisorderKristen Barbour, Matthew N Bainbridge, Kristen Wigby, et al.
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