Fuz Mutant Mice Reveal Shared Mechanisms between Ciliopathies and FGF-Related Syndromes

A global double‐fluorescent Cre reporter mouse

Mandar D. Muzumdar, Bosiljka Tasic, Kazunari Miyamichi et al. · genesis · 2007 · 3.7K citations · Full text

Life Sciences, Cell Biology, Genetics +14

A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells

Christian Schulz, Elisa Gomez Perdiguero, Laurent Chorro et al. · Science · 2012 · 2.5K citations

Life Sciences, Biology, Cell Biology +13

Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase

Paul S. Danielian, David Muccino, David H. Rowitch et al. · Current Biology · 1998 · 1.3K citations · Full text

Medicine, Genetics, Molecular Genetics +17

New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

Philip L. Beales, Nursel Elçioğlu, Adrian S. Woolf et al. · Journal of Medical Genetics · 1999 · 972 citations · Full text

Medicine, Genetics, Pediatrics +9

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge et al. · Nature Genetics · 1995 · 937 citations

Life Sciences, Genetics, Molecular Genetics +7