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المؤلفون: Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Manjusha S Ghosh, Bart J H Dequeker, Florence Perold, Claire Kastner, Emmanuelle Kieffer, Ingrid Segers, Alexander Gheldof, Frederik J Hes, Karen Sermon, Willem Verpoest, Stéphane Viville
المساهمون: Clinical sciences, Centre for Medical Genetics, Brussels Heritage Lab, Medical Genetics, Faculty of Medicine and Pharmacy, Basic (bio-) Medical Sciences, UZB Other, Reproduction and Genetics, Centre for Reproductive Medicine - Gynaecology
المصدر: Human reproduction update.
مصطلحات موضوعية: systematic review, Reproductive Medicine, female infertility, reproductive genetics, medically assisted reproduction, monogenic, Obstetrics and Gynecology, Genetics(clinical), gene–disease relationship, clinical validation, Art, differences in sex development
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a01fda61779bee7a38846cbe437b21c
https://pubmed.ncbi.nlm.nih.gov/36571510 -
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المؤلفون: Emmanuelle Kieffer, Philippe Gosset, Nathalie Gardes, Claire Kastner, Jean-Christophe Nicod, Céline Moutou
المصدر: Reproductive BioMedicine Online. 36:e37
مصطلحات موضوعية: Genetics, Reproductive Medicine, Genetic counseling, Obstetrics and Gynecology, De novo mutation, Biology, Developmental Biology
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المؤلفون: Catherine Celebi, Claire Kastner, Jean-Christophe Nicod, Céline Moutou, C. Rongieres, Olivier Pirrello, Nathalie Gardes, Emmanuelle Kieffer, Philippe Gosset, Isabelle Koscinski, Nicolas Becker
المصدر: European journal of human genetics : EJHG. 24(2)
مصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Heterozygote, FRAX, Genotype, Biology, Primary Ovarian Insufficiency, Preimplantation genetic diagnosis, Article, Loss of heterozygosity, 03 medical and health sciences, Fragile X Mental Retardation Protein, 0302 clinical medicine, Trinucleotide Repeats, Pregnancy, Genetics, medicine, Humans, Allele, Genetics (clinical), Alleles, Preimplantation Diagnosis, 030219 obstetrics & reproductive medicine, Obstetrics, medicine.disease, FMR1, Fragile X syndrome, 030104 developmental biology, Fragile X Syndrome, Mutation, Microsatellite, Female, Single-Cell Analysis, Multiplex Polymerase Chain Reaction, Microsatellite Repeats