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Susan M Gribble

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Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 7, 2005
SmartCapture and the frontiers of FISH technology: report of the Digital Scientific UK SmartCapture User's Meeting, Peterhouse College Cambridge, UK, 2nd September 2005Alistair G Reid, Susan M Gribble
Nature Protocols|November 7, 2009
Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarraysSusan M Gribble, Bee Ling Ng, Elena Prigmore, et al.
European Journal of Human Genetics : EJHG|August 25, 2005
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individualsJulia Baptista, Elena Prigmore, Susan M Gribble, et al.
Plos One|February 21, 2012
Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis mediaStephanie Kuhn, Neil Ingham, Selina Pearson, et al.
Genes, Chromosomes & Cancer|June 12, 2003
Genomic imbalances in CML blast crisis: 8q24.12-q24.13 segment identified as a common region of over-representationSusan M Gribble, Alistair G Reid, Ian Roberts, et al.
American Journal of Human Genetics|March 29, 2008
Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohortJulia Baptista, Catherine Mercer, Elena Prigmore, et al.
Human Molecular Genetics|March 16, 2004
Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangementSandra Rodríguez-Perales, Bárbara Meléndez, Susan M Gribble, et al.
Genome Biology|May 15, 2008
Finishing the finished human chromosome 22 sequenceCharlotte G Cole, Owen T McCann, John E Collins, et al.
Human Genetics|January 6, 2006
Micro-array analyses decipher exceptional complex familial chromosomal rearrangementChristine Fauth, Susan M Gribble, Keith M Porter, et al.
European Journal of Medical Genetics|July 24, 2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic stateÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|December 7, 2005
SmartCapture and the frontiers of FISH technology: report of the Digital Scientific UK SmartCapture User's Meeting, Peterhouse College Cambridge, UK, 2nd September 2005Alistair G Reid, Susan M Gribble
Nature Protocols|November 7, 2009
Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarraysSusan M Gribble, Bee Ling Ng, Elena Prigmore, et al.
European Journal of Human Genetics : EJHG|August 25, 2005
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individualsJulia Baptista, Elena Prigmore, Susan M Gribble, et al.
Plos One|February 21, 2012
Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis mediaStephanie Kuhn, Neil Ingham, Selina Pearson, et al.
Genes, Chromosomes & Cancer|June 12, 2003
Genomic imbalances in CML blast crisis: 8q24.12-q24.13 segment identified as a common region of over-representationSusan M Gribble, Alistair G Reid, Ian Roberts, et al.
American Journal of Human Genetics|March 29, 2008
Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohortJulia Baptista, Catherine Mercer, Elena Prigmore, et al.
Human Molecular Genetics|March 16, 2004
Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangementSandra Rodríguez-Perales, Bárbara Meléndez, Susan M Gribble, et al.
Genome Biology|May 15, 2008
Finishing the finished human chromosome 22 sequenceCharlotte G Cole, Owen T McCann, John E Collins, et al.
Human Genetics|January 6, 2006
Micro-array analyses decipher exceptional complex familial chromosomal rearrangementChristine Fauth, Susan M Gribble, Keith M Porter, et al.
European Journal of Medical Genetics|July 24, 2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic stateÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Pageof 2