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Journal of Perinatology : Official Journal of the California Perinatal Association|May 31, 2020
Genetic testing strategies in the newbornJeanne Carroll, Kristen Wigby, Sarah Murray
American Journal of Medical Genetics. Part A|December 15, 2018
A novel autosomal dominant mutation in SOX18 resulting in a fatal case of hypotrichosis-lymphedema-telangiectasia syndromeHannah Wangberg, Kristen Wigby, Marilyn C Jones
Journal of the American Academy of Child and Adolescent Psychiatry|March 6, 2019
Whole Exome Sequencing Guides Pharmacotherapy for an Adolescent With Autism Spectrum Disorder and PsychosisKristen Wigby, Samuel Nicolas, Matthew Carpinello, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 18, 2020
Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysisKristen Wigby, Lisa Cordeiro, Rebecca Wilson, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 28, 2024
Clinical utility of rapid whole genome sequencing in neonatal patients receiving extracorporeal membrane oxygenation (ECMO)Milan D Amin, Kristen Wigby, Denise Suttner, et al.
American Journal of Medical Genetics. Part A|September 20, 2016
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosisKristen Wigby, Cheryl D'Epagnier, Susan Howell, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|February 22, 2022
Activated phosphoinositide 3-kinase δ syndrome associated with nephromegaly, growth hormone deficiency, bronchiectasis: a case reportMegan Craig, Bob Geng, Kristen Wigby, et al.
Child Neurology Open|August 16, 2021
To Be or No B2: A Rare Cause of Stridor and Weakness in a ToddlerAliya L Frederick, Jennifer H Yang, Sarah Schneider, et al.
Cold Spring Harbor Molecular Case Studies|May 28, 2017
Rapid whole-genome sequencing identifies a novel homozygous <i>NPC1</i> variant associated with Niemann-Pick type C1 disease in a 7-week-old male with cholestasisAmber Hildreth, Kristen Wigby, Shimul Chowdhury, 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.
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