SCO-ping Out the Mechanisms Underlying the Etiology of Hydrocephalus

Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1)

(2010) D. F. Callen et al.   CLINICAL GENETICS

The Oak Ridge Polycystic Kidney mouse: Modeling ciliopathies of mice and men

(2008) Jonathan M. Lehman et al.   DEVELOPMENTAL DYNAMICS

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

(2008) Russell J. Ferland et al.   HUMAN MOLECULAR GENETICS

Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages

(2008) P. Dietrich et al.   HUMAN MOLECULAR GENETICS

Mutations inHydinimpair ciliary motility in mice

(2008) Karl-Ferdinand Lechtreck et al.   JOURNAL OF CELL BIOLOGY

Distinct Isoforms of the RFX Transcription Factor DAF-19 Regulate Ciliogenesis and Maintenance of Synaptic Activity

(2008) Gabriele Senti et al.   MOLECULAR BIOLOGY OF THE CELL

Foxj1 transcription factors are master regulators of the motile ciliogenic program

(2008) Xianwen Yu et al.   NATURE GENETICS

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

(2008) Nicola Brunetti-Pierri et al.   NATURE GENETICS