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Cell|March 15, 2020
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer VariantsEvgeny Z Kvon, Yiwen Zhu, Guy Kelman, et al.
The Lancet Regional Health. Europe|November 24, 2025
Management and survival of patients with cancer of unknown primary discussed by a French national multidisciplinary tumour board: a retrospective analysisCélia Dupain, Nicolas Jacquin, Aurélien Latouche, et al.
Journal of Medical Genetics|November 29, 2012
EFTUD2 haploinsufficiency leads to syndromic oesophageal atresiaChristopher T Gordon, Florence Petit, Myriam Oufadem, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Duplication of 10q24 locus: broadening the clinical and radiological spectrumMuriel Holder-Espinasse, Aleksander Jamsheer, Fabienne Escande, et al.
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