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Browsing by Author Nolan, Patrick

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Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Author(s)Bogani, Debora; Willoughby, Catherine; Davies, Jennifer, et al
TypeJournal article
Date Published2005
Date Created-

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Author(s)Curtin, John A; Quint, Elizabeth; Tsipouri, Vicky, et al
TypeJournal article
Date Published2003
Date Created-

New Semidominant Mutations that affect Mouse Development

Author(s)Bogani, Debora; Warr, Nick; Elms, Paul, et al
TypeJournal article
Date Published2004
Date Created-

Stringent requirement of a proper level of canonical WNT signalling activity for head formation in mouse embryo

Author(s)Fossat, Nicolas; Jones, Vanessa; Khoo, Poh-Lynn, et al
TypeJournal article
Date Published2011
Date Created-
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