prof. dr. Paul Coucke
Show
Sort by
-
- Journal Article
- A1
- open access
Accurate quantification of homologous recombination in zebrafish : brca2 deficiency as a paradigm
-
A novel case of autosomal dominant cutis laxa in a consanguineous family : report and literature review
-
- Journal Article
- A1
- open access
GLUT10 - lacking in arterial tortuosity syndrome - is localized to the endoplasmic reticulum of human fibroblasts
-
Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome
-
A mild form of Stickler syndrome type II caused by mosaicism of COL11A1
-
Congenital contractural arachnodactyly : delineation of clinical criteria
-
Myhre syndrome : broadening the phenotypic spectrum
-
Zebrafish modeling of the β4GalT7-deficient type of Ehlers-Danlos syndrome
-
Congenital contractural arachnodactyly : delineation of clinical criteria
-
Myhre syndrome : broadening the phenotypic spectrum