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BeSHG CFTR - 2012
BeSHG Cytogenetics Final Draft - 2011
BeSHG FMR-1 - 2012
BeSHG FRAX Final Draft - 2011
BeSHG HBOC - 2012
BeSHG NIPT Incidental Findings - 2016
BeSHG Postnatal Karyotype - 2012
BeSHG Prenatal Array - 2013
EuroGentest NGS Final Draft v2 - 2014
European best practice CFTR - European Journal of Human Genetics
Genetic breast and ovarian cancer predisposition-FR
Genetic testing and common disorders in a public helath care
Genetic testing in asymptomatic minors
KCE Birt-Hogg-Dube
KCE Cowden syndrome
KCE FAMM
KCE FAP
KCE Hereditary breast cancer
KCE Li Fraumeni syndrome
KCE Lynch syndrome
KCE MEN1
KCE MEN2
KCE Neurofibromatosis type1
KCE Neurofibromatosis type2
KCE Paraganglioma-Phaeochromocytoma
KCE vonHippel-Lindau
NIPT good clinical practice - 2017
VKGN Informing relatives in hereditary predisposition to cancer - NL
Whole-genome sequencing in health care
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