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

Bogani, D; Willoughby, C; Davies, J; Kaur, K; Mirza, G; Paudyal, A; Haines, H; ... Arkell, RM; + view all (2005) Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 102 (35) pp. 12477-12482. 10.1073/pnas.0500584102.

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Type: Article
Title: Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
DOI: 10.1073/pnas.0500584102
Keywords: Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, anophthalmia, ENU mutagenesis, holoprosencephaly, MUTATION CONGENITAL-HYDROCEPHALUS, FORKHEAD/WINGED-HELIX GENE, ETHYL-N-NITROSOUREA, CHROMOSOME 6P, MICE, MUTAGENESIS, SCHIZOPHRENIA, LOCUS, MF1, ABNORMALITIES
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Ophthalmology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science > Centre for Cardiovascular Genetics
URI: http://discovery.ucl.ac.uk/id/eprint/1459733
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