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Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
August 9, 2003
Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH)
Louise V Hills, Sara Nouri, Howard R Slater
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
August 4, 2004
Centric fission--simple and complex mechanisms
Jo Perry, Howard R Slater, K H Andy Choo
Journal of the Association of Genetic Technologists
|
June 2, 2015
Detection of segmental chromosome copy number gains by improved fluorescence in situ hybridization techniques
Nicole L Chia, Howard R Slater, Julia M Potter
JAMA Neurology
|
June 10, 2014
Methylation analysis in newborn screening for fragile X syndrome
David E Godler, David J Amor, Howard R Slater
Molecular Cytogenetics
|
May 13, 2008
An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)
Mahmoud S Khaniani, Paul Kalitsis, Trent Burgess, et al.
American Journal of Medical Genetics. Part A
|
August 15, 2006
Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome
Peter Kannu, Paul Oei, Howard R Slater, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2010
Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome
David E Godler, Howard R Slater, David Amor, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2005
A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndrome
Tiong Yang Tan, Agnes Bankier, Howard R Slater, et al.
European Journal of Medical Genetics
|
September 24, 2009
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment
Alison Yeung, Damien Bruno, Ingrid E Scheffer, et al.
Plos One
|
February 24, 2018
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies
Claudine M Kraan, Kim M Cornish, Quang M Bui, et al.
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of 5
Search research articles
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Showing results (1-10 of 43) with videos related to
Sort By:
Page
of 5
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
August 9, 2003
Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH)
Louise V Hills, Sara Nouri, Howard R Slater
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
August 4, 2004
Centric fission--simple and complex mechanisms
Jo Perry, Howard R Slater, K H Andy Choo
Journal of the Association of Genetic Technologists
|
June 2, 2015
Detection of segmental chromosome copy number gains by improved fluorescence in situ hybridization techniques
Nicole L Chia, Howard R Slater, Julia M Potter
JAMA Neurology
|
June 10, 2014
Methylation analysis in newborn screening for fragile X syndrome
David E Godler, David J Amor, Howard R Slater
Molecular Cytogenetics
|
May 13, 2008
An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)
Mahmoud S Khaniani, Paul Kalitsis, Trent Burgess, et al.
American Journal of Medical Genetics. Part A
|
August 15, 2006
Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome
Peter Kannu, Paul Oei, Howard R Slater, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 15, 2010
Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome
David E Godler, Howard R Slater, David Amor, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2005
A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndrome
Tiong Yang Tan, Agnes Bankier, Howard R Slater, et al.
European Journal of Medical Genetics
|
September 24, 2009
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment
Alison Yeung, Damien Bruno, Ingrid E Scheffer, et al.
Plos One
|
February 24, 2018
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies
Claudine M Kraan, Kim M Cornish, Quang M Bui, et al.
Page
of 5