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European Journal of Medical Genetics|November 8, 2019
Split hand/foot malformation associated with 20p12.1 deletion: A case reportLyse Ruaud, Ricarda Flöttmann, Malte Spielmann, et al.
BMC Medical Genetics|June 16, 2019
Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literatureChamara Sampath Paththinige, Nirmala Dushyanthi Sirisena, Fabienne Escande, et al.
Anticancer Research|July 29, 2016
Lack of Relationship Between Clinical Features and KRAS Mutations in Patients with Metastatic Colorectal CancerAnne Ploquin, Farid Zerimech, Fabienne Escande, et al.
Neurosurgical Review|December 1, 2021
Progestin-related WHO grade II meningiomas behavior-a single-institution comparative case seriesAntoine Devalckeneer, Rabih Aboukais, Maxime Faisant, et al.
European Journal of Medical Genetics|February 22, 2011
A familial syndromal form of omphaloceleMarylin Port-Lis, Camille Leroy, Sylvie Manouvrier, et al.
Targeted Oncology|November 3, 2023
Histo-Molecular Factors of Response to Combined Chemotherapy and Immunotherapy in Non-Small Cell Lung CancersMarine Marchal, Vincent Leroy, Hélène Behal, et al.
Neuro-Oncology Practice|March 9, 2026
High-grade gliomas and Lynch syndrome: A retrospective descriptive study with a literature reviewHugo Duprez, Apolline Monfilliette, Marie Csanyi, et al.
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