Author/Creator: ffrench-Constant, C - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator ffrench-Constant, C

1. Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11–17 distinct from the GAP related domain. Issue 4 (1st April 2004)

Authors:: Mattocks, C; Baralle, D; Tarpey, P; ffrench-Constant, C; Bobrow, M; Whittaker, J
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 4(2004)
Page Start:: e48
Record Type:: Journal Article
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2. Identification of a mutation that perturbs NF1 agene splicing using genomic DNA samples and a minigene assay. Issue 3 (1st March 2003)

Authors:: Baralle, M; Baralle, D; De Conti, L; Mattocks, C; Whittaker, J; Knezevich, A; ffrench-Constant, C; Baralle, F E
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 3(2003)
Page Start:: 220
Record Type:: Journal Article
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3. Myoclonic movement disorder associated with microdeletion of chromosome 22q11. Issue 5 (1st November 2002)

Authors:: Baralle, D; Trump, D; ffrench-Constant, C; Dick, D J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 73:Issue 5(2002)
Page Start:: 600
Record Type:: Journal Article
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4. Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer). Issue 6 (3rd June 2005)

Authors:: Whittaker, J L; Mattocks, C; Baralle, D; Tarpey, P; ffrench-Constant, C; Bobrow, M
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 6(2005)
Page Start:: e33
Record Type:: Journal Article
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5. Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer). Issue 7 (1st July 2005)

Authors:: Whittaker, J L; Mattocks, C; Baralle, D; Tarpey, P; ffrench-Constant, C; Bobrow, M
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 7(2005)
Page Start:: e41
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗