Torthaí cuardaigh - Alexandre Moerman
- 1 - 3 toradh as 3 á dtaispeáint
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1
Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children de réir Gaëlle Bougeard, Françoise Charbonnier, Alexandre Moerman, Cosette Martin, Marie Madeleine Ruchoux, Nathalie Drouot, Thierry Frébourg
Foilsithe / Cruthaithe 2003Carta -
2
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 de réir Catherine Dodé, Luís Teixeira, Jacqueline Levilliers, Corinne Fouveaut, Philippe Bouchard, Marie-Laure Kottler, James Lespinasse, Anne Lienhardt-Roussie, Michèle Mathieu, Alexandre Moerman, Graeme Morgan, Arnaud Murat, Jean-Edmont Toublanc, Sławomir Wołczyński, Marc Delpech, Christine Petit, Jacques Young, Jean-Pierre Hardelin
Foilsithe / Cruthaithe 2006Artigo -
3
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age de réir Sandra Mercier, Annick Toutain, Aurélie Toussaint, Martine Raynaud, Claire De Barace, Pascale Marcorelles, Laurent Pasquier, Martine Blayau, Caroline Espil, P. Parent, Hubert Journel, Leïla Lazaro, Jon Andoni Urtizberea, Alexandre Moerman, Laurence Bonhomme‐Faivre, B. Eymard, Kim Maincent, Romain K. Gherardi, Denys Chaigne, Rabah Ben Yaou, France Leturcq, Jamel Chelly, Isabelle Desguerre
Foilsithe / Cruthaithe 2013Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Internal medicine
Medicine
Biology
Disease
Gene
Genetics
Pathology
Age of onset
Anosmia
Brain tumor
Coronavirus disease 2019 (COVID-19)
Duchenne muscular dystrophy
Dystrophin
Endocrinology
Genetic counseling
Hormone
Hypogonadotropic hypogonadism
Infectious disease (medical specialty)
Kallmann syndrome
Lymphoma
Missense mutation
Muscular dystrophy
Mutation
Oncology
Phenotype
Point mutation