Bettina Lorenz

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

Fiona Francis, Steffen Hennig, Bernd Korn et al. · Nature Genetics · 1995 · 1.1K citations

Genetic Disorder, Genetics, X–linked Hypophosphatemic Rickets +3

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

Víctor L. Ruiz‐Pérez, Susan Ide, Tim M. Strom et al. · Nature Genetics · 2000 · 350 citations

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +7

Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia

Tim M. Strom, Fiona Francis, Bettina Lorenz et al. · Human Molecular Genetics · 1997 · 199 citations

Genomic Organization of the Human <i>PEX</i> Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets

Fiona Francis, Tim M. Strom, Steffen Hennig et al. · Genome Research · 1997 · 162 citations · Full text

Genetics, Genomic Mechanism, Molecular Biology +19

Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene

Bettina Lorenz · Human Molecular Genetics · 1998 · 90 citations · Full text