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American Journal of Obstetrics and Gynecology|January 10, 2023
Cytogenetic outcomes following a failed cell-free DNA screen: a population-based retrospective cohort study of 35,146 singleton pregnanciesKara Bellai-Dussault, Lynn Meng, Heather Howley, et al.
The Journal of Allergy and Clinical Immunology|February 8, 2005
CD40 and OX40 ligand are increased on stimulated asthmatic airway smooth muscleJanette K Burgess, Anita E Blake, Sarah Boustany, et al.
Molecular and Cellular Biology|February 6, 2013
A high-confidence interaction map identifies SIRT1 as a mediator of acetylation of USP22 and the SAGA coactivator complexSean M Armour, Eric J Bennett, Craig R Braun, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 2, 2017
Sex differences in parent-reported executive functioning and adaptive behavior in children and young adults with autism spectrum disorderEmily I White, Gregory L Wallace, Julia Bascom, et al.
BMJ Military Health|October 19, 2021
Social and economic costs of gambling problems and related harm among UK military veteransShaun Harris, R D Pockett, G Dighton, et al.
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|March 27, 2015
Magnetic nanoparticle hyperthermia enhances radiation therapy: A study in mouse models of human prostate cancerAnilchandra Attaluri, Sri Kamal Kandala, Michele Wabler, et al.
Human Molecular Genetics|September 23, 2010
Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's diseaseMarian C Aldhous, Suhaili Abu Bakar, Natalie J Prescott, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 4, 2021
Performance of a universal prenatal screening program incorporating cell-free fetal DNA analysis in Ontario, CanadaShelley D Dougan, Nan Okun, Kara Bellai-Dussault, et al.
Electrophoresis|September 1, 1995
Mutation processes at human minisatellitesA J Jeffreys, M J Allen, J A Armour, et al.
Neurogenetics|January 18, 2006
PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1Patricia Combes, Marie-Noelle Bonnet-Dupeyron, Fernande Gauthier-Barichard, et al.
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