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R SLATER

Showing results (381-390 of 414) with videos related to

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Genomics|December 7, 2007
The ascent of cat breeds: genetic evaluations of breeds and worldwide random-bred populationsMonika J Lipinski, Lutz Froenicke, Kathleen C Baysac, et al.
Human Molecular Genetics|January 12, 2013
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubertyDavid E Godler, Yoshimi Inaba, Elva Z Shi, et al.
Blood|June 25, 1999
Complete remission of t(11;17) positive acute promyelocytic leukemia induced by all-trans retinoic acid and granulocyte colony-stimulating factorJ H Jansen, M C de Ridder, W M Geertsma, et al.
Clinical Chemistry|January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot studyDavid E Godler, Howard R Slater, Quang M Bui, et al.
Medical and Pediatric Oncology|November 1, 1996
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumorsM Mannens, M Alders, B Redeker, et al.
American Journal of Human Genetics|June 30, 2012
Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregatesKatsiaryna Belaya, Sarah Finlayson, Clarke R Slater, et al.
Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
Clinical Genetics|October 3, 2009
Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonismD Z Loesch, M S Khaniani, H R Slater, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2011
Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonismDanuta Z Loesch, David E Godler, Andrew Evans, et al.
Pageof 42

Showing results (381-390 of 414) with videos related to

Sort By:
Pageof 42
Genomics|December 7, 2007
The ascent of cat breeds: genetic evaluations of breeds and worldwide random-bred populationsMonika J Lipinski, Lutz Froenicke, Kathleen C Baysac, et al.
Human Molecular Genetics|January 12, 2013
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubertyDavid E Godler, Yoshimi Inaba, Elva Z Shi, et al.
Blood|June 25, 1999
Complete remission of t(11;17) positive acute promyelocytic leukemia induced by all-trans retinoic acid and granulocyte colony-stimulating factorJ H Jansen, M C de Ridder, W M Geertsma, et al.
Clinical Chemistry|January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot studyDavid E Godler, Howard R Slater, Quang M Bui, et al.
Medical and Pediatric Oncology|November 1, 1996
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumorsM Mannens, M Alders, B Redeker, et al.
American Journal of Human Genetics|June 30, 2012
Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregatesKatsiaryna Belaya, Sarah Finlayson, Clarke R Slater, et al.
Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
Clinical Genetics|October 3, 2009
Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonismD Z Loesch, M S Khaniani, H R Slater, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2011
Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonismDanuta Z Loesch, David E Godler, Andrew Evans, et al.
Pageof 42