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

Maryse Bonduelle

Showing results (21-30 of 54) with videos related to

Pageof 6
Sort By:
American Journal of Medical Genetics. Part A|May 9, 2015
Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndromePieter Verdyck, Veerle Berckmoes, Anick De Vos, et al.
Human Reproduction (Oxford, England)|June 5, 2009
A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosisKathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
Human Reproduction (Oxford, England)|March 1, 2002
Neonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999)Maryse Bonduelle, Inge Liebaers, Veerle Deketelaere, et al.
Human Reproduction (Oxford, England)|September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parametersMaryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Reproductive Biomedicine Online|September 24, 2020
Follow-up in the field of reproductive medicine: an ethical explorationVerna Jans, Wybo Dondorp, Maryse Bonduelle, et al.
Molecular Genetics & Genomic Medicine|September 4, 2021
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrheaAsma Sassi, Julie Désir, Sarah Duerinckx, et al.
Mutation Research|April 21, 2007
Loss of nuclear BRCA1 protein staining in normal tissue cells derived from BRCA1 and BRCA2 mutation carriersSylvia De Brakeleer, Marika Bogdani, Jacques De Grève, et al.
Fertility and Sterility|February 6, 2003
Prenatal genetic testing by amniocentesis appears to result in a lower risk of fetal loss than chorionic villus sampling in singleton pregnancies achieved by intracytoplasmic sperm injectionEfstratios Kolibianakis, Kaan Osmanagaoglu, Luc De Catte, et al.
Nucleic Acids Research|October 21, 2015
DIDA: A curated and annotated digenic diseases databaseAndrea M Gazzo, Dorien Daneels, Elisa Cilia, et al.
Human Reproduction (Oxford, England)|November 4, 2011
Neonatal follow-up of 995 consecutively born children after embryo biopsy for PGDS Desmyttere, M De Rycke, C Staessen, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|May 9, 2015
Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndromePieter Verdyck, Veerle Berckmoes, Anick De Vos, et al.
Human Reproduction (Oxford, England)|June 5, 2009
A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosisKathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
Human Reproduction (Oxford, England)|March 1, 2002
Neonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999)Maryse Bonduelle, Inge Liebaers, Veerle Deketelaere, et al.
Human Reproduction (Oxford, England)|September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parametersMaryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Reproductive Biomedicine Online|September 24, 2020
Follow-up in the field of reproductive medicine: an ethical explorationVerna Jans, Wybo Dondorp, Maryse Bonduelle, et al.
Molecular Genetics & Genomic Medicine|September 4, 2021
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrheaAsma Sassi, Julie Désir, Sarah Duerinckx, et al.
Mutation Research|April 21, 2007
Loss of nuclear BRCA1 protein staining in normal tissue cells derived from BRCA1 and BRCA2 mutation carriersSylvia De Brakeleer, Marika Bogdani, Jacques De Grève, et al.
Fertility and Sterility|February 6, 2003
Prenatal genetic testing by amniocentesis appears to result in a lower risk of fetal loss than chorionic villus sampling in singleton pregnancies achieved by intracytoplasmic sperm injectionEfstratios Kolibianakis, Kaan Osmanagaoglu, Luc De Catte, et al.
Nucleic Acids Research|October 21, 2015
DIDA: A curated and annotated digenic diseases databaseAndrea M Gazzo, Dorien Daneels, Elisa Cilia, et al.
Human Reproduction (Oxford, England)|November 4, 2011
Neonatal follow-up of 995 consecutively born children after embryo biopsy for PGDS Desmyttere, M De Rycke, C Staessen, et al.
Pageof 6