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Publications by Marie Legendre
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia
American Journal of Human Genetics
Genetics
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus
American Journal of Human Genetics
Genetics
Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance
American Journal of Human Genetics
Genetics
Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation
Frontiers in Endocrinology
Endocrinology
Metabolism
Diabetes
Bi-Allelic Missense ABCA3 Mutations in a Patient With Childhood ILD Who Reached Adulthood
ERJ Open Research
Pulmonary
Respiratory Medicine
COPA Syndrome as a Cause of Lupus Nephritis
Kidney International Reports
Nephrology
Critical Evaluation of Sinonasal Disease in 64 Adults With Primary Ciliary Dyskinesia
Journal of Clinical Medicine
