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المؤلفون: Christine E. M. de Die-Smulders, Klaske D. Lichtenbelt, A. Titia Lely, Jos Dreesen, Franka E. van Reekum, Cindy E. Simcox, Theodora C. van Tilborg, Rozemarijn Snoek, Marijn Stokman, Albertien M. van Eerde, Nine V A M Knoers, Aimee D C Paulussen
المساهمون: MUMC+: DA KG Lab Centraal Lab (9), RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica
المصدر: Clin J Am Soc Nephrol
Clinical journal of the American Society of Nephrology, 15(9), 1279-1286. American Society of Nephrology
Clinical Journal of the American Society of Nephrology, 15(9), 1279-1286. AMER SOC NEPHROLOGYمصطلحات موضوعية: ESHRE PGD, Male, Pediatrics, Epidemiology, 030232 urology & nephrology, Nephritis, Hereditary, Reproductive technology, Disease, Critical Care and Intensive Care Medicine, 0302 clinical medicine, MARKERS, Pregnancy, Risk Factors, Netherlands, RISK, OUTCOMES, 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, genetic renal disease, Polycystic Kidney, Autosomal Dominant, Autosomal Recessive Polycystic Kidney Disease, FAMILY, Nephrology, Female, Kidney Diseases, Live birth, Adult, medicine.medical_specialty, Reproductive Techniques, Assisted, BIRTH, Autosomal dominant polycystic kidney disease, Genetic Counseling, DIAGNOSIS, Young Adult, 03 medical and health sciences, Predictive Value of Tests, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Preimplantation Diagnosis, ADPKD, Polycystic Kidney, Autosomal Recessive, Retrospective Studies, Genetic testing, Transplantation, MEDICINE, business.industry, Editorials, Retrospective cohort study, Original Articles, medicine.disease, Mutation, business, Alport syndrome, Kidney disease
وصف الملف: application/pdf
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المؤلفون: Aimee D C Paulussen, Christine E. M. de Die-Smulders, N. D. Muntjewerff, Frank J.M. Broekmans, Marieke van Deursen-Luijten, John J.M. Engelen, Yvonne Arens, Jos Dreesen, M. Meijer-Hoogeveen, Aafke P.A. van Montfoort, Malou Heijligers, Edith Coonen, Mark A. H. B. M. van der Hoeven, Katelijne Bouman, Ron J. T. van Golde, I. Homminga, Andrea Peeters, Vyne van der Schoot
المساهمون: MUMC+: KIO Kemta (9), RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Obstetrie & Gynaecologie, MUMC+: DA KG Lab Centraal Lab (9), RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Klinische Genetica, MUMC+: VMK IVF Lab (9), MUMC+: MA Medische Staf Obstetrie Gynaecologie (9), Kindergeneeskunde, MUMC+: MA Medische Staf Kindergeneeskunde (9)
المصدر: Journal of Assisted Reproduction and Genetics, 35(11), 1995-2002. Springer
Journal of Assisted Reproduction and Genetics
Journal of Assisted Reproduction and Genetics, 35(11), 1995-2002. SPRINGER/PLENUM PUBLISHERSمصطلحات موضوعية: Male, Time Factors, Abortion, 0302 clinical medicine, Pregnancy, Prospective Studies, 030212 general & internal medicine, Assisted Reproduction Technologies, Child, Children, Genetics (clinical), Congenital malformations, OUTCOMES, 030219 obstetrics & reproductive medicine, NEWBORNS, Obstetrics, Follow-up, Incidence (epidemiology), Preimplantation genetic diagnosis, Obstetrics and Gynecology, General Medicine, Perinatal Care, Gestation, Female, MISDIAGNOSIS, medicine.symptom, Adult, medicine.medical_specialty, Birth weight, Reproductive medicine, Congenital Abnormalities, 03 medical and health sciences, ESHRE PGD CONSORTIUM, PREGNANCIES, Genetics, medicine, Humans, Genetic Testing, Diagnostic Errors, Preimplantation Diagnosis, METAANALYSIS, Fetus, ANEUPLOIDY, business.industry, Infant, Newborn, Perinatal outcome, BLASTOMERE, BIRTH-WEIGHT, Low birth weight, Reproductive Medicine, HUMAN EMBRYOS, business, Follow-Up Studies, Developmental Biology
وصف الملف: application/pdf
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المؤلفون: Veerle Goossens, Filipa Carvalho, Jos Dreesen, Eftychia Dimitriadou, Daniela Zuccarello, Martine De Rycke, Céline Moutou, Georgia Kakourou, Nathalie Vermeulen, Carles Giménez
المساهمون: Reproduction and Genetics, Basic (bio-) Medical Sciences, Medical Genetics, RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Lab Centraal Lab (9)
المصدر: Human Reproduction Open
Human reproduction open, 2020(3):018, 1-18. Oxford University Pressمصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Good Practice, Best practice, ESHRE, good practice, mitochondrial DNA, monogenic disorders, exclusion testing, 03 medical and health sciences, 0302 clinical medicine, Medicine, Medical physics, Genetics(clinical), Good practice, pathogenic variants, Genetic testing, 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, structural chromosomal aberrations, business.industry, Diagnostic test, Embryo biopsy, Aneuploidy, ESHRE Pages, Clinical Practice, HLA, 030104 developmental biology, PRACTICE GUIDELINES, numerical chromosomal aberrations, business, preimplantation genetic testing
وصف الملف: Electronic-eCollection
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المؤلفون: Jessie Theuns, Katrien Omer François, Han G. Brunner, Masoud Zamani Esteki, Edith Coonen, Thierry Voet, Joris Vermeesch, Dennis Lorson, Cindy Melotte, Rebecca Richards, Olga Tšuiko, Sophie Debrock, Marion Drüsedau, Aspasia Destouni, Karen Peeraer, Scott Happe, Jos Dreesen, Aimee D C Paulussen, Kasper W.J. Derks, Benoit Devogelaere, Jeroen Meekels, Eftychia Dimitriadou, Josien G. Derhaag, Chris M. J. van Uum, Joke Allemeersch, Heleen Masset, Christine E. M. de Die-Smulders
المساهمون: RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Lab Centraal Lab (9), Obstetrie & Gynaecologie, MUMC+: VMK IVF Lab (9), Genetica & Celbiologie, MUMC+: DA Klinische Genetica (5), Klinische Genetica, MUMC+: DA KG Polikliniek (9)
المصدر: Human Reproduction, 34(8), 1608-1619. Oxford University Press
مصطلحات موضوعية: 0301 basic medicine, Computer science, Concordance, Single-nucleotide polymorphism, Computational biology, DIAGNOSIS, INHERITANCE, Genome, DNA sequencing, Embryo Culture Techniques, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, FERTILIZATION, medicine, Humans, Genetic Testing, Preimplantation Diagnosis, Genetic testing, PGD, 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, Rehabilitation, Haplotype, High-Throughput Nucleotide Sequencing, Obstetrics and Gynecology, 030104 developmental biology, COPY-NUMBER, Haplotypes, Reproductive Medicine, Data quality, Female, SNP array
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المؤلفون: Edith Coonen, J.P.M. Geraedts, J.L.H. Evers, M. Bras, John C.M. Dumoulin, Jos Dreesen
المصدر: Scopus-Elsevier
Europe PubMed Centralمصطلحات موضوعية: Blastomeres, medicine.medical_specialty, Biopsy, Cleavage Stage, Ovum, Fertilization in Vitro, Biology, Preimplantation genetic diagnosis, Andrology, Embryonic and Fetal Development, Internal medicine, medicine, Humans, Magnesium, Blastocyst, Biopsy procedure, Preimplantation Diagnosis, medicine.diagnostic_test, Rehabilitation, Embryogenesis, Obstetrics and Gynecology, Embryo, Blastomere, Free medium, Culture Media, Endocrinology, medicine.anatomical_structure, Reproductive Medicine, Evaluation Studies as Topic, embryonic structures, Calcium, Female
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المؤلفون: Vivianne C. G. Tjan-Heijnen, Herman Tournaye, I.A.P. Derks-Smeets, Pieter Verdyck, Willem Verpoest, Shari Mackens, Jos Dreesen, Ron J. T. van Golde, Christine E. M. de Die-Smulders, Maryse Bonduelle, Joep P.M. Geraedts, Martine De Rycke, Aimee D C Paulussen, M. Meijer-Hoogeveen, Jacques De Greve
المساهمون: Biology of the Testis, Gyneacology-Urology, Reproductive immunology and implantation, Surgical clinical sciences, Medical Genetics, Reproduction and Genetics, Laboratory for Medical and Molecular Oncology, Department of Embryology and Genetics, RS: GROW - Developmental Biology, Promovendi ODB, Genetica & Celbiologie, Klinische Genetica, Interne Geneeskunde, RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, RS: GROW - R4 - Reproductive and Perinatal Medicine
المصدر: Vrije Universiteit Brussel
Breast Cancer Research and Treatment, 145(3), 673-681. Springer, Chamمصطلحات موضوعية: Male, Cancer Research, medicine.medical_treatment, GUIDELINES, Pregnancy, Prenatal Diagnosis, skin and connective tissue diseases, RISK, Ovarian Neoplasms, medicine.diagnostic_test, BRCA1 Protein, Preimplantation genetic diagnosis, Pregnancy Outcome, WOMEN, ASSOCIATION, respiratory system, Oncology, lipids (amino acids, peptides, and proteins), Female, Infertility, Adult, medicine.medical_specialty, Hereditary breast and ovarian cancer, Breast Neoplasms, INFERTILITY, Breast cancer, ESHRE PGD CONSORTIUM, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, METAANALYSIS, Preimplantation Diagnosis, Genetic testing, Gynecology, BRCA2 Protein, In vitro fertilisation, BRCA2 MUTATION, business.industry, medicine.disease, BRCA1, BRCA2, Reproductive outcome, Asymptomatic Diseases, Ovarian cancer, business, FOLLOW-UP, Asymptomatic carrier
وصف الملف: application/pdf