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Soins. Pediatrie, Puericulture|March 27, 2018
[Mother-baby follow-up at home and the welcome of the baby in the family]Florence Petit-Lacroix, Christine Garcia-Valadier
Nature Reviews. Genetics|February 7, 2017
Limb development: a paradigm of gene regulationFlorence Petit, Karen E Sears, Nadav Ahituv
Malaria Journal|June 9, 2016
Sub-Saharan red cell antigen phenotypes and glucose-6-phosphate dehydrogenase deficiency variants in French GuianaFlorence Petit, Pascal Bailly, Jacques Chiaroni, et al.
European Journal of Medical Genetics|April 27, 2024
PRKD1-related telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome: Case report and review of the literatureFiona Leduc, Thomas Smol, Benoit Catteau, et al.
European Journal of Medical Genetics|November 19, 2021
Performance of meta-predictors for the classification of MED13L missense variations, implication of raw parametersThomas Smol, Frédéric Frénois, Sylvie Manouvrier-Hanu, et al.
Ophthalmic Genetics|October 22, 2019
Pigmented paravenous chorioretinal atrophy revealing a chronic granulomatous diseaseVasily M Smirnov, Delphine Ley, Brigitte Nelken, et al.
Clinical Genetics|July 17, 2025
Humeroradial Synostosis: An Updated Classification and Differential Diagnosis Based on Genetic AetiologyFiona Leduc, Clémence Vanlerberghe, Fabienne Escande, et al.
European Journal of Human Genetics : EJHG|August 26, 2018
The radial expansion of the Diego blood group system polymorphisms in Asia: mark of co-migration with the Mongol conquestsFlorence Petit, Francesca Minnai, Jacques Chiaroni, et al.
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