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Developmental Cognitive Neuroscience|November 15, 2025
Preterm birth, socioeconomic status, and white matter development across childhoodKatie Mckinnon, Manuel Blesa Cábez, Melissa Thye, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2021
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosisZerin Hyder, Eduardo Calpena, Yang Pei, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020
SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.Clinical Epigenetics|March 26, 2024
Epigenetic scores of blood-based proteins as biomarkers of general cognitive function and brain healthHannah M Smith, Joanna E Moodie, Karla Monterrubio-Gómez, et al.Journal of Community Genetics|July 1, 2026
Rare disease genomics and justice: overview of a workshop at the Fondation Brocher, 22-24 January 2025Angus Clarke, Ruth Horn, Elena Avram, et al.Journal of Medical Genetics|August 3, 2006
STK11 status and intussusception risk in Peutz-Jeghers syndromeN Hearle, V Schumacher, F H Menko, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 19, 2006
Frequency and spectrum of cancers in the Peutz-Jeghers syndromeNicholas Hearle, Valérie Schumacher, Fred H Menko, et al.International Forum of Allergy & Rhinology|May 9, 2025
The Development and Validation of the Smell-Qx Questionnaire, Based on a Systematic Review of the Literature and the COMET Initiative on the Development of Core Outcome Sets for Clinical Trials in Olfactory DisordersMatt Lechner, Alexander Fjaeldstad, Umar Rehman, et al.Nature Biomedical Engineering|December 23, 2024
Leucine zipper-based immunomagnetic purification of CAR T cells displaying multiple receptorsScott E James, Sophia Chen, Brandon D Ng, et al.Diabetologia|May 1, 2026
Psychosocial implications, acceptability and ethics of screening for paediatric type 1 diabetes: a systematic review and mixed methods evidence synthesisLauren M Quinn, David Stanley, Francesca Milano, et al.Pageof 144