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P Stanier

Showing results (61-70 of 76) with videos related to

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Genomics|June 1, 1991
Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator geneF Tata, P Stanier, C Wicking, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defectsK Doudney, J Grinham, J Whittaker, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 21, 2006
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weightS Apostolidou, S Abu-Amero, K O'Donoghue, et al.
The EMBO Journal|June 1, 1988
Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant winglessB J Wainwright, P J Scambler, P Stanier, et al.
Clinical Genetics|July 13, 2012
X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutationsE Pauws, E Peskett, C Boissin, et al.
Genomics|January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3S A Forbes, L Brennan, M Richardson, et al.
Human Genetics|January 8, 2015
Genome-wide methylation analysis in Silver-Russell syndrome patientsA R Prickett, M Ishida, S Böhm, et al.
Clinical Genetics|December 6, 2017
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephalyM Ishida, T Cullup, C Boustred, et al.
Human Molecular Genetics|March 15, 2006
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and humanD Monk, R Sanches, P Arnaud, et al.
Nature|April 6, 1987
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsX Estivill, M Farrall, P J Scambler, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Genomics|June 1, 1991
Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator geneF Tata, P Stanier, C Wicking, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defectsK Doudney, J Grinham, J Whittaker, et al.
Journal of Molecular Medicine (Berlin, Germany)|December 21, 2006
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weightS Apostolidou, S Abu-Amero, K O'Donoghue, et al.
The EMBO Journal|June 1, 1988
Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant winglessB J Wainwright, P J Scambler, P Stanier, et al.
Clinical Genetics|July 13, 2012
X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutationsE Pauws, E Peskett, C Boissin, et al.
Genomics|January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3S A Forbes, L Brennan, M Richardson, et al.
Human Genetics|January 8, 2015
Genome-wide methylation analysis in Silver-Russell syndrome patientsA R Prickett, M Ishida, S Böhm, et al.
Clinical Genetics|December 6, 2017
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephalyM Ishida, T Cullup, C Boustred, et al.
Human Molecular Genetics|March 15, 2006
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and humanD Monk, R Sanches, P Arnaud, et al.
Nature|April 6, 1987
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsX Estivill, M Farrall, P J Scambler, et al.
Pageof 8