Multiple mutations in mouse Chd7 provide models for CHARGE syndrome-Reference-Cited by-同舟云学术

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Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

Published:2005-10-03 Issue:22 Volume:14 Page:3463-3476
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bosman Erika A.,Penn Andrew C.,Ambrose John C.,Kettleborough Ross,Stemple Derek L.,Steel Karen P.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/22/3463/17242039/ddi375.pdf

Reference66 articles.

1. Alavizadeh, A., Kiernan, A.E., Nolan, P., Lo, C., Steel, K.P. and Bucan, M. (2001) The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects. Dev. Biol., 234, 244–260.

2. Kiernan, A.E., Erven, A., Voegeling, S., Peters, J., Nolan, P., Hunter, J., Bacon, Y., Steel, K.P., Brown, S.D. and Guenet, J.L. (2002) ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis. Mamm. Genome, 13, 142–148.

3. Hawker, K., Fuchs, H., Angelis, M.H. and Steel, K.P. (2005) Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4. Int. J. Audiol., 44, 171–177.

4. Pau, H., Hawker, K., Fuchs, H., De Angelis, M.H. and Steel, K.P. (2004) Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation. Otol. Neurotol., 25, 707–713.

5. Nolan, P.M., Sollars, P.J., Bohne, B.A., Ewens, W.J., Pickard, G.E. and Bucan, M. (1995) Heterozygosity mapping of partially congenic lines: mapping of a semidominant neurological mutation, Wheels (Whl), on mouse chromosome 4. Genetics, 140, 245–254.

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