Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Laïla El Khattabi

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Fertility and Sterility|April 4, 2013
Is intracytoplasmic morphologically selected sperm injection effective in patients with infertility related to teratozoospermia or repeated implantation failure?Laïla El Khattabi, Charlotte Dupont, Nathalie Sermondade, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|August 25, 2014
Could sperm grade under high magnification condition predict IMSI clinical outcome?Christophe Sifer, Laïla El Khattabi, Charlotte Dupont, et al.
Prenatal Diagnosis|March 6, 2024
Performance of cell-free DNA testing for common fetal trisomies in triplet pregnanciesHoda Zakaria, Pascale Kleinfinger, Laurence Lohmann, et al.
Communications Biology|January 28, 2025
Chromatin environment-dependent effects of DOT1L on gene expression in male germ cellsManon Coulée, Alberto de la Iglesia, Mélina Blanco, et al.
Birth Defects Research|July 9, 2024
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicismEmmanuelle Pannier, Abel Sekri, Nathalie Roux, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
American Journal of Human Genetics|July 8, 2021
Optical genome mapping enables constitutional chromosomal aberration detectionTuomo Mantere, Kornelia Neveling, Céline Pebrel-Richard, et al.
Journal of Medical Genetics|August 20, 2025
Resolving structural variations missed by short-read sequencing uncovers their pathogenicityCaroline Schluth-Bolard, Laïla El Khattabi, Pierre-Antoine Rollat-Farnier, et al.
Annales D'Endocrinologie|September 11, 2021
Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome)Sophie Christin-Maitre, Maria Givony, Frédérique Albarel, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature reviewLaïla El Khattabi, Sylvie Jaillard, Joris Andrieux, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Fertility and Sterility|April 4, 2013
Is intracytoplasmic morphologically selected sperm injection effective in patients with infertility related to teratozoospermia or repeated implantation failure?Laïla El Khattabi, Charlotte Dupont, Nathalie Sermondade, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|August 25, 2014
Could sperm grade under high magnification condition predict IMSI clinical outcome?Christophe Sifer, Laïla El Khattabi, Charlotte Dupont, et al.
Prenatal Diagnosis|March 6, 2024
Performance of cell-free DNA testing for common fetal trisomies in triplet pregnanciesHoda Zakaria, Pascale Kleinfinger, Laurence Lohmann, et al.
Communications Biology|January 28, 2025
Chromatin environment-dependent effects of DOT1L on gene expression in male germ cellsManon Coulée, Alberto de la Iglesia, Mélina Blanco, et al.
Birth Defects Research|July 9, 2024
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicismEmmanuelle Pannier, Abel Sekri, Nathalie Roux, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
American Journal of Human Genetics|July 8, 2021
Optical genome mapping enables constitutional chromosomal aberration detectionTuomo Mantere, Kornelia Neveling, Céline Pebrel-Richard, et al.
Journal of Medical Genetics|August 20, 2025
Resolving structural variations missed by short-read sequencing uncovers their pathogenicityCaroline Schluth-Bolard, Laïla El Khattabi, Pierre-Antoine Rollat-Farnier, et al.
Annales D'Endocrinologie|September 11, 2021
Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome)Sophie Christin-Maitre, Maria Givony, Frédérique Albarel, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature reviewLaïla El Khattabi, Sylvie Jaillard, Joris Andrieux, et al.
Pageof 2