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Journal of Assisted Reproduction and Genetics|December 21, 2024
Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1Charlotte Sonigo, Noémie Ranisavljevic, Mathilde Guigui, et al.
American Journal of Human Genetics|February 16, 2022
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermiaZine-Eddine Kherraf, Caroline Cazin, Amine Bouker, et al.
Microbiology Resource Announcements|June 22, 2019
Discovery and Characterization of Bacteriophage LuckyBarnesSavannah L Underwood, Amanda Foto, Amanda F Ray, et al.
Development (Cambridge, England)|November 18, 2021
CFAP61 is required for sperm flagellum formation and male fertility in human and mouseSiyu Liu, Jintao Zhang, Zine Eddine Kherraf, et al.
Human Reproduction (Oxford, England)|October 18, 2019
CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case reportJulie Beurois, Guillaume Martinez, Caroline Cazin, et al.
American Journal of Human Genetics|March 15, 2011
DPY19L2 deletion as a major cause of globozoospermiaIsabelle Koscinski, Elias Elinati, Camille Fossard, et al.
Chest|January 1, 1976
Open pulmonary biopsy. Nineteen-year experience with 416 consecutive operationsJ F Ray, B R Lawton, W O Myers, et al.
Nature Genetics|April 17, 2007
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertilityKlaus Dieterich, Ricardo Soto Rifo, Anne Karen Faure, et al.
American Journal of Human Genetics|April 16, 2013
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermiaThassadite Dirami, Baptiste Rode, Mathilde Jollivet, et al.
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