Jill Urquhart and Mutations - Free people check

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Novel PEX11B Mutations Extend the Peroxisome Biogenesis ...

eprints.whiterose.ac.uk

by RL Taylor · · Cited by 17 — Rachel L. Taylor,1 Mark T. Handley,2 Sarah Waller,3 Christopher Campbell,3 Jill Urquhart,1 Alison. M. Meynert,2 Jamie M. Ellingford, › ...

Mutations in LZTR1 add to the complex heterogeneity of...

www.scienceopen.com

... Daly, J.E. Urquhart, A. Fryer, C.F. Rustad, S.J. Mills, A. Samii, D. Du Plessis, D. Halliday, S. Barbarot, F. Bourdeaut, W.G. Newman, D.G. Evans, Jill Urquhart.

Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome,...

www.ncbi.nlm.nih.gov

Dan Hanson,1,2 Philip G. Murray,1,2,3 James O'Sullivan,2,3 Jill Urquhart,2,3 Sarah Daly,2,3 Sanjeev S. Bhaskar,2,3 Leslie G. Biesecker,4,5 ...

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway...

www.ncbi.nlm.nih.gov

Emma M.M. Burkitt Wright,1,13 Helen L. Spencer,1,13 Sarah B. Daly,1 Forbes D.C. Manson,1 Leo A.H. Zeef,2 Jill Urquhart,1 Nicoletta Zoppi,3 ...

LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and...

www.biomedsearch.com

... Jill Urquhart; Boi-Dinh Chung; Samira Ismail; Khalda Amr; Ayca D Aslanger; Christian Becker; Christian Netzer; Pete Scambler; Wafaa Eyaid; Hanan Hamamy;

All web results to the name "Jill Urquhart"

LRP4 mutations alter Wnt/beta-catenin signaling and cause ...

read.qxmd.com

... Asim Cenani, Jill Urquhart, Boi-Dinh Chung, Samira Ismail, Khalda Amr, Ayca D Aslanger, Christian Becker, Christian Netzer, Pete Scambler, Wafaa Eyaid, ... › read › lrp4-mutations-alter-wn...

Novel PEX11B Mutations Extend the Peroxisome Biogenesis ...

www.research.ed.ac.uk

Rachel L Taylor, Mark T Handley, Sarah Waller, Christopher Campbell, Jill Urquhart, Alison M Meynert, Jamie M Ellingford, Deirdre Donnelly, Gisela Wilcox, ... Tracy A Briggs, Gillian I Rice, Sarah Daly, Jill Urquhart, Hannah Gornall, Brigitte Bader-Meunier, Kannan Baskar, Shankar Baskar, Veronique Baudouin, ... › fingerprints

Molecular Vision: Identification of seven novel ZNF469 mutations in...

www.molvis.org

Burkitt Wright, Helen L. Spencer, Sarah B. Daly, Forbes D.C. Manson, Leo A.H. Zeef, Jill Urquhart, Nicoletta Zoppi, Richard Bonshek, Ioannis ...

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway...

research.rug.nl

author = "Wright, {Emma M. M. Burkitt} and Spencer, {Helen L.} and Daly, {Sarah B.} and Manson, {Forbes D. C.} and Zeef, {Leo A. H.} and Jill Urquhart and ...

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