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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 criteria for starting genetic analysis
HBOC management criteria
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
MTHFR polymorphism testing_ENG_guidelines_2019
MTHFR polymorphism testing_FR_guidelines_2019
MTHFR polymorphism testing_NL_guidelines_2019
Test génétiques en accès direct-Statement College
VKGN Informing relatives in hereditary predisposition to cancer - NL
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