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BeSHG CFTR - 2012
BeSHG FMR-1 - 2012
BeSHG Postnatal Karyotype - 2012
BeSHG prenatal consortium_guidelines for NIPT good clinical practice
BeSHG prenatal consortium_guidelines for fetal genome-wide sequencing (NGS) in ongoing pregnancies
BeSHG prenatal consortium_guidelines for prenatal rasopathy panel
BeSHG prenatal consortium_guidelines managing incidental findings detected by NIPT
BeSHG prenatal consortium_guidelines prenatal array
BeSHG prenatal consortium_table susceptibility loci
COVID19_WHO_Laboratory biosafety
COVID19_lijst prioriteiten klinische genetica_NL
COVID19_liste priorités en génétique clinique_FR
ESHG recommendations_Genetic testing and common disorders in a public health care
ESHG recommendations_Genetic testing in asymptomatic minors
ESHG recommendations_Whole-genome sequencing in health care
EuroGentest NGS_2014
European best practice CFTR - European Journal of Human Genetics
European guidelines for rare hereditary cancer predisposition syndromes
Genetische zelftests-Statement College
HBOC Belgian guideline for diagnostic testing criteria
HBOC management guidelines
KCE Birt-Hogg-Dube
KCE Cowden syndrome
KCE Hereditary breast cancer
KCE Li Fraumeni syndrome
KCE Lynch syndrome
KCE Neurofibromatosis type1
KCE Neurofibromatosis type2
KCE Paraganglioma-Phaeochromocytoma
KCE vonHippel-Lindau
Lynch syndrome_Guidelines by FAPA
MTHFR polymorphism testing_ENG_guidelines_2019
MTHFR polymorphism testing_FR_guidelines_2019
MTHFR polymorphism testing_NL_guidelines_2019
Pancreatic cancer - Belgian guideline for diagnostic testing criteria
Prostate cancer, hereditary - testing guidelines
SMA carrier testing indications
Test génétiques en accès direct-Statement College
VKGN Informing relatives in hereditary predisposition to cancer - NL