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Prostate cancer susceptibility (HOXB13 - hot spot mutation p.(Gly84Glu))
HOXB13
Familial prostate cancer
Centre de Génétique Humaine - CHU Sart-Tilman
Prostate cancer
HOXB13
Familial prostate cancer
Centre de Génétique Médicale UCL
Temple syndrome / Kagami-Ogata Syndrome
DLK1
,
MEG3
,
RTL1
Temple syndrome due to maternal uniparental disomy of chromosome 14
,
Temple syndrome due to paternal 14q32.2 hypomethylation
,
Temple syndrome due to paternal 14q32.2 microdeletion
,
Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14
,
Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation
,
Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion
Centre de Génétique Médicale UCL
Protein S deficiency
PROS1
Severe hereditary thrombophilia due to congenital protein S deficiency
Centrum Medische Genetica - UZ Gent
ABCB1 genotyping (c.3435C>T, c.1199G>A ) - Transport protein - Pharmacogenetics
ABCB1
Resistance to colchicine
Centre de Génétique Médicale UCL
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