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1 . Academic Journal
Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
저자
by
Patel, Chirag
;
Cooper-Charles, Lisa
;
McMullan, Dominic J.
;
Walker, Judith M.
;
Davison, Val
, et al.
소스
European Journal of Human Genetics
. Jun2011, Vol. 19 Issue 6, p634-639. 6p. 1 Black and White Photograph, 1 Diagram, 1 Chart.
Web of Science
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7 . Academic Journal
Characterization of a 3;6 translocation associated with renal cell carcinoma.
저자
by
Foster, Rebecca E.
;
Abdulrahman, Mahera
;
Morris, Mark R.
;
Prigmore, Elena
;
Gribble, Susan
, et al.
소스
Genes, Chromosomes & Cancer; Apr2007, Vol. 46 Issue 4, p311-317, 7p
Web of Science
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7 . Academic Journal
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
저자
by
Wordsworth, Sarah
;
Buchanan, James
;
Regan, Regina
;
Davison, Val
;
Smith, Kim
, et al.
소스
Genomic Medicine; Jan2007, Vol. 1 Issue 1/2, p35-45, 11p
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7 . Academic Journal
Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma
저자
by
Chughtai, Shaheen A.
;
Genus, Tracey
;
Ramani, Pramila
;
Dyer, Sara
;
Powell, Judy E.
, et al.
소스
European Journal of Cancer
. Aug2006, Vol. 42 Issue 12, p1826-1834. 9p.
Full Text (ScienceDirect)
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7 . Academic Journal
Microarray Based Analysis of 3p25-p26 Deletions (3p- Syndrome)
저자
by
Shuib, Salwati
;
McMullan, Dominic
;
Rattenberry, Eleanor
;
Barber, Richard M.
;
Rahman, Fatimah
, et al.
소스
American Journal Of Medical Genetics - A
. Oct 01, 2009 149A(10):2099-2105
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7 .
MOESM11 of Immunostaining of modified histones defines high-level features of the human metaphase epigenome
저자
by
Terrenoire, Edith
;
McRonald, Fiona
;
Halsall, John
;
Page, Paula
;
Illingworth, Robert
, et al.
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Open Access (OpenAIRE)
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7 .
of Immunostaining of modified histones defines high-level features of the human metaphase epigenome
저자
by
Terrenoire, Edith
;
McRonald, Fiona
;
Halsall, John
;
Page, Paula
;
Illingworth, Robert
, et al.
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7 . Academic Journal
Confirmation of FWT1 as a Wilms’ tumour susceptibility gene and phenotypic characteristics of Wilms’ tumour attributable to FWT1.
저자
by
Rahman, N.
;
Abidi, Fatima
;
Ford, Deborah
;
Arbour, Laura
;
Rapley, Elizabeth
, et al.
소스
Human Genetics; Nov1998, Vol. 103 Issue 5, p547-556, 10p
Full Text (Springer)
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7 . Periodical
Microarray based analysis of 3p25p26 deletions 3p syndromeHow to cite this article: Shuib S, McMullan D, Rattenberry E, Barber RM, Rahman F, Zatyka M, Chapman C, Macdonald F, Latif F, Davison V, Maher ER. 2009. Microarray based analysis of 3p25p26 deletions 3p syndrome. Am J Med Genet Part A 149A:2099–2105.
저자
by
Shuib, Salwati
;
McMullan, Dominic
;
Rattenberry, Eleanor
;
Barber, Richard M.
;
Rahman, Fatimah
, et al.
소스
American Journal of Medical Genetics. Part A; October 2009, Vol. 149 Issue: 10 p2099-2105, 7p
Web of Science
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7 . Periodical
Genomic Imbalances in Pediatric Intracranial Ependymomas Define Clinically Relevant Groups
저자
by
Dyer, Sara
;
Prebble, Emma
;
Davison, Val
;
Davies, Paul
;
Ramani, Pramila
, et al.
소스
American Journal of Pathology; December 2002, Vol. 161 Issue: 6 p2133-2141, 9p
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