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Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.American Journal of Human Genetics|October 25, 2011
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19Cecilie Bredrup, Sophie Saunier, Machteld M Oud, et al.Cancers|July 20, 2021
Evaluation of Integrated HPV DNA as Individualized Biomarkers for the Detection of Recurrent CIN2/3 during Post-Treatment SurveillanceHeike Hoyer, Grit Mehlhorn, Cornelia Scheungraber, et al.Journal of Environmental Management|February 26, 2022
Identifying barriers for nature-based solutions in flood risk management: An interdisciplinary overview using expert community approachPavel Raška, Nejc Bezak, Carla S S Ferreira, et al.Gut|July 18, 2000
The Vienna classification of gastrointestinal epithelial neoplasiaR J Schlemper, R H Riddell, Y Kato, et al.Psychology & Health|February 20, 2016
Implementation intention and planning interventions in Health Psychology: Recommendations from the Synergy Expert Group for research and practiceMartin S Hagger, Aleksandra Luszczynska, John de Wit, et al.European Journal of Human Genetics : EJHG|January 16, 2014
Myhre and LAPS syndromes: clinical and molecular review of 32 patientsCaroline Michot, Carine Le Goff, Clémentine Mahaut, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
GUÍA: a digital platform to facilitate result disclosure in genetic counselingSabrina A Suckiel, Jaqueline A Odgis, Katie M Gallagher, et al.Nature Genetics|February 8, 2005
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndromeIrene A Aligianis, Colin A Johnson, Paul Gissen, et al.Human Mutation|February 1, 2011
MLL2 mutation spectrum in 45 patients with Kabuki syndromeAimée D C Paulussen, Alexander P A Stegmann, Marinus J Blok, et al.Pageof 149