Ralf Spörle

The mouse <i>Pax2</i> ^1Neu mutation is identical to a human <i>PAX2</i> mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

Jack Favor, Rodica Sandulache, A. Neuhäuser-Klaus et al. · Proceedings of the National Academy of Sciences · 1996 · 391 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The Expression of the MouseZic1, Zic2,andZic3Gene Suggests an Essential Role forZicGenes in Body Pattern Formation

Takeharu Nagai, Jun Aruga, Shinji Takada et al. · Developmental Biology · 1997 · 319 citations

Life Sciences, Genetics, Molecular Genetics +14

Multiple roles for neurofibromin in skeletal development and growth

Mateusz Kolanczyk, Nadine Kossler, Jirko Kühnisch et al. · Human Molecular Genetics · 2007 · 135 citations · Full text

Medicine, Developmental Biology, Pathology +17

Computer-based three-dimensional visualization of developmental gene expression

Johannes Streicher, Markus A. Donat, Bernhard Strauss et al. · Nature Genetics · 2000 · 93 citations

Life Sciences, Developmental Biology, Molecular Biology +14

Characterization and Expression Pattern of thefrizzledGeneFzd9,the Mouse Homolog ofFZD9Which Is Deleted in Williams–Beuren Syndrome

Yu-Ker Wang, Ralf Spörle, Tamar Paperna et al. · Genomics · 1999 · 82 citations

Life Sciences, Genetics, Molecular Genetics +17