نتائج البحث - Jos Dreesen
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1
ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders† حسب Filipa Carvalho, Céline Moutou, Eftychia Dimitriadou, Jos Dreesen, Carles Giménez, V. Goossens, Georgia Kakourou, Nathalie Vermeulen, Daniela Zuccarello, Martine De Rycke
منشور في 2020Artigo -
2
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres حسب Maartje C. van Rij, Marjan De Rademaeker, Céline Moutou, Jos Dreesen, Martine De Rycke, Inge Liebaers, Joep P.M. Geraedts, C E de Die-Smulders, Stéphane Viville
منشور في 2011Artigo -
3
Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study حسب Jos Dreesen, Aspasia Destouni, Georgia Kourlaba, Birte Degn, Mette Wulf Christensen, Filipa Carvalho, Céline Moutou, Sioban SenGupta, Seema Dhanjal, Pamela Renwick, S. Davies, Emmanouel Kanavakis, G. Harton, Joanne Traeger‐Synodinos
منشور في 2013Artigo -
4
BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD حسب I. A. P. Derks-Smeets, Theodora C van Tilborg, Aafke P.A. van Montfoort, Luc Smits, Helen L. Torrance, M. Meijer‐Hoogeveen, Frank J. Broekmans, Jos Dreesen, Aimée Paulussen, Vivianne C. G. Tjan‐Heijnen, Irene Homminga, Merel M.J. van den Berg, Margreet G.E.M. Ausems, Martine De Rycke, Christine de Die‐Smulders, Willem Verpoest, R. van Golde
منشور في 2017Artigo -
5
Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss حسب Rick Essers, И. Н. Лебедев, Ants Kurg, Е. А. Фонова, Servi J.C. Stevens, Rebekka M. Koeck, Ulrike von Rango, Lloyd Brandts, Spyridon Panagiotis Deligiannis, Nikitina Tv, Е. А. Саженова, Е. Н. Толмачева, А. А. Кашеварова, D. A. Fedotov, Viktoria V. Demeneva, Д. И. Жигалина, Г.В. Дроздов, Salwan Al‐Nasiry, Merryn Macville, Arthur van den Wijngaard, Jos Dreesen, Aimée Paulussen, Alexander Hoischen, Han G. Brunner, Andres Salumets, Masoud Zamani Esteki
منشور في 2023Artigo -
6
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing حسب A Janssen, Rebekka M. Koeck, Rick Essers, Ping Cao, Wanwisa van Dijk, Marion Drüsedau, Jeroen Meekels, Burcu Yaldiz, Maartje van de Vorst, Bart de Koning, Debby M.E.I. Hellebrekers, Servi J.C. Stevens, Su Ming Sun, Malou Heijligers, Sonja A. de Munnik, Chris M.J. van Uum, Juul Achten, Lars Hamers, Marjan Naghdi, Lisenka E.L.M. Vissers, Ron J T van Golde, Guido de Wert, Jos Dreesen, Christine de Die‐Smulders, Edith Coonen, Han G. Brunner, Arthur van den Wijngaard, Aimée Paulussen, Masoud Zamani Esteki
منشور في 2024Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Medicine
Gene
Genetic testing
Gynecology
Internal medicine
Pregnancy
Preimplantation genetic diagnosis
Andrology
Genotype
Obstetrics
Best practice
Clinical Practice
Computational biology
Concordance
DNA
DNA sequencing
Deep sequencing
Embryo
Engineering
Engineering ethics
Family medicine
First trimester
Genome
Genotyping
Gestation
Good practice
In vitro fertilisation
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