Liesbeth M. Bleeker-Wagemakers

Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

Albert de la Chapelle, Ritva Tolvanen, Gudrun Boysen et al. · Nature Genetics · 1992 · 175 citations

Tyrosine Substitution, Alzheimer's Disease, Biochemistry +5

Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population

S. van Soest, L. Ingeborgh van den Born, Andreas Gal et al. · Genomics · 1994 · 119 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

A. Gal, B. Wieringa, D F Smeets et al. · Cytogenetic and Genome Research · 1986 · 74 citations

Genetics, Pathology, Molecular Genetics +17

Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome

Andreas Gal, Christine Stolzenberger, Thomas F. Wienker et al. · Clinical Genetics · 1985 · 54 citations

Close Linkage, Genetic Disorder, X Chromosome +7

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

Liesbeth M. Bleeker-Wagemakers, Ursula Friedrich, A. Gal et al. · Human Genetics · 1985 · 52 citations

Chromatin, Close Linkage, Developmental Biology +10