Alfons García-Piñero

SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

Naresh K. Hanchate, Paolo Giacobini, Pierre Lhuillier et al. · PLoS Genetics · 2012 · 210 citations · Full text

A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

Julie Sarfati, Anne Guiochon‐Mantel, Philippe Rondard et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 145 citations