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Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|March 15, 2020
Global warming and planetary health: An open letter to the WHO from scientific and indigenous people urging for paleo-microbiology studiesP Charlier, G Héry-Arnaud, Y Coppens, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
Translational Psychiatry|April 9, 2020
Machine learning classification of ADHD and HC by multimodal serotonergic dataA Kautzky, T Vanicek, C Philippe, et al.
European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.
Journal of Autism and Developmental Disorders|December 21, 2006
Development of a video-based evaluation tool in Rett syndromeS Fyfe, J Downs, O McIlroy, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 30, 2021
Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutationsM Theiler, L Weibel, S Christen-Zaech, et al.
Physical Review Letters|September 29, 2023
Tuning the Multiferroic Properties of BiFeO_{3} under Uniaxial StrainP Hemme, J-C Philippe, A Medeiros, et al.
Revue Des Maladies Respiratoires|January 6, 2020
[A case of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) syndrome]A Moussa Ounteini, A Aziagbe Koffi, S Rabiou, et al.
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