Genomic imprinting and Silver-Russell syndrome : candidate genes on chromosome 7

Genomic imprinting and Silver-Russell syndrome : candidate genes on chromosome 7

Bibliographic Details
Main Author:	Wakeling, Emma Louise
Published:	University College London (University of London) 1999
Subjects:	572.8 SRS
Online Access:	http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325386

Similar Items

Identification of candidate regulatory regions for insulin-like growth factor-2 imprinting on mouse distal chromosome 7
by: Davies, K. R.
Published: (2000)

Genomic imprinting and the aetiology of human chromosome abnormalities
by: James, Rowena Sarah
Published: (1995)

Investigation of candidate imprinted tumour suppressor genes
by: Judson, Hannah
Published: (2001)

Molecular analysis of the imprinted domain at chromosome 7q32 : a candidate region for Silver-Russell syndrome
by: Bentley, Louise
Published: (2003)

Identification and analysis of imprinted and non-imprinted genes in distal human chromosome 20q13
by: Morán Barroso, Verónica Fabiola
Published: (2001)

Evolution and gene regulation of the genomic imprinting mechanism
by: Mungall, Andrew James
Published: (2007)

The Gnas imprinting cluster : identification and analysis of candidate regulatory elements
by: Coombes, C.
Published: (2003)

The isolation and testing of candidate genes for DiGeorge syndrome
by: Taylor, Catherine Louise
Published: (1997)

The identificaiton and characterisation of novel imprinted genes
by: Wood, Andrew James
Published: (2007)

Mapping the Plasmodium falciparum genome with yeast artificial chromosomes
by: Meaney, Paul James
Published: (1995)

The evolution of genomic imprinting : a comparative analysis of the DLK1/DIO3 domain in extant vertebrates
by: Edwards, C. A.
Published: (2008)

Imprinting of X-chromosome inactivation and functional studies of the regulation of Xist promoter activity in preimplantation embryos and transgenic mice
by: Goto, Tetsuya
Published: (1998)

Candidate genes for X-linked mental retardation syndromes
by: Feldman, Eleanor J.
Published: (1993)

Molecularly imprinted polymers for protome analysis
by: Bonini, Francesca
Published: (2008)

Novel monomer-template assemblies for molecular imprinting
by: Jupe, Hannah Rachel Elizabeth
Published: (2007)

Chromosomal engineering to produce a model of human 5q-syndrome
by: Holmes, L. R.
Published: (2006)

Investigation of possible cloning hosts for mammalian artificial chromosomes
by: Mann, Kathryn Louise
Published: (2000)

Gene conversion on the human Y chromosome
by: Bowden, Georgina Rebecca
Published: (2011)

Characterisation of the TSCI candidate region on human chromosome 9q34
by: Woodward, Karen Jane
Published: (1995)

The selection and analysis of multiple SNPs in candidate genes
by: Butler, Joe Matthew
Published: (2009)

Investigation of the role of chromosome 7 in human cell immortalisation and cancer
by: Berrington, Mary
Published: (1999)

Chromatin organisation at differentially methylated regions of imprinted mouse loci
by: Gregory, R. I.
Published: (2001)

New Applications For Molecularly Imprinted Polymers in Fluorescence Assays and Sensors
by: Hunt, Claire Elizabeth
Published: (2006)

Genome studies of human chromosome 22q13.3
by: Smink, Lukas-Jan
Published: (2000)

Detecting genes for developmental dyslexia on chromosome 6p
by: Cope, Natalie Alexandra
Published: (2006)

A study of spontaneous and 5-fluorodeoxyuridine induced chromosomal instability and its significance in the sheep (Ovis aries) genome
by: Ê¿AliÌ„, AhÌ£mad
Published: (2001)

Genomic organisation of a repeat sequence island on the mouse X chromosome
by: Mileham, P. J. R.
Published: (1997)

Construction and integration of genome maps of domestic dog chromosome X and 1
by: Spriggs, Helen Florence
Published: (2000)

Interacting functions of reciprocally expressed imprinted transcripts from the mouse Gnas locus
by: Dickins, B. J. A.
Published: (2007)

The characterisation of genes localised on chromosome 2p23.3
by: Wightman, Patrick John
Published: (2001)

The role of condensin in chromosome resolution
by: Charbin, A. A.
Published: (2012)

Disease-associated balanced chromosomal rearrangements : molecular characterisation of two cases, with a review of the impact of published cases in human genetic research
by: Harewood, Louise
Published: (2006)

Identification of a silencing element at the imprinted H19 locus using mouse and Drosophila transgenes
by: Brenton, J. D.
Published: (2001)

Statistical methods for linkage disequilibrium mapping of disease susceptibility genes in candidate regions
by: Chapman, J. M.
Published: (2005)

The search for candidate genes in asthma and atopy
by: Wilkinson, Jane Elizabeth
Published: (1998)

Physical mapping of human chromosomal band Iq21 and characterisation of new genes
by: Lioumi, Maria
Published: (2000)

The structure and organisation of the genome of human herpesvirus-6 (strain U1102) and identification of a candidate immediate early gene locus
by: Thomson, Brian James
Published: (1991)

Molecular genetic analysis of chromosome 22q in ovarian cancer
by: Bryan, Emma Jane
Published: (1998)

Modelling Chromosome Behaviour in Space and Time
by: Penfold, Christopher Andrew
Published: (2009)

Investigations into chromosome-specific susceptibilities to aneuploidy
by: Bourner, R. D. P.
Published: (1998)