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H Fiegler

Showing results (11-20 of 19) with videos related to

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Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Journal of Medical Genetics|February 27, 2004
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardationI Rost, H Fiegler, C Fauth, et al.
Journal of Medical Genetics|October 4, 2005
Prenatal detection of unbalanced chromosomal rearrangements by array CGHL Rickman, H Fiegler, C Shaw-Smith, et al.
Journal of Medical Genetics|September 10, 2003
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarraysH Fiegler, S M Gribble, D C Burford, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 27, 2004
Applications of combined DNA microarray and chromosome sorting technologiesS M Gribble, H Fiegler, D C Burford, et al.
Journal of Medical Genetics|February 4, 2005
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?R Redon, M Rio, S G Gregory, et al.
Oncogene|May 17, 2006
A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGHR Roylance, P Gorman, T Papior, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Journal of Medical Genetics|January 7, 2005
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesS M Gribble, E Prigmore, D C Burford, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Journal of Medical Genetics|February 27, 2004
Tetrasomy 21pter-->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardationI Rost, H Fiegler, C Fauth, et al.
Journal of Medical Genetics|October 4, 2005
Prenatal detection of unbalanced chromosomal rearrangements by array CGHL Rickman, H Fiegler, C Shaw-Smith, et al.
Journal of Medical Genetics|September 10, 2003
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarraysH Fiegler, S M Gribble, D C Burford, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 27, 2004
Applications of combined DNA microarray and chromosome sorting technologiesS M Gribble, H Fiegler, D C Burford, et al.
Journal of Medical Genetics|February 4, 2005
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?R Redon, M Rio, S G Gregory, et al.
Oncogene|May 17, 2006
A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGHR Roylance, P Gorman, T Papior, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Journal of Medical Genetics|January 7, 2005
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesS M Gribble, E Prigmore, D C Burford, et al.
Pageof 2