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W Scherer

Showing results (351-360 of 915) with videos related to

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Molecular Genetics & Genomic Medicine|October 20, 2021
Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testingIskra Peltekova, Afiqah Yusuf, Jennifer Frei, et al.
Journal of Genetic Counseling|September 7, 2020
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditionsAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
BMC Medical Genetics|May 8, 2020
Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerAnna Bobyn, Mehdi Zarrei, Yuankun Zhu, et al.
Respiration Physiology|March 1, 1993
Microemboli reduce phase III slopes of CO2 and invert phase III slopes of infused SF6M S Schreiner, L G Leksell, S R Gobran, et al.
Blood|May 1, 1996
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasiaE J Johnson, S W Scherer, L Osborne, et al.
Diabetes|March 29, 2005
Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics StudyAndrew P Boright, Andrew D Paterson, Lucia Mirea, et al.
Risk Analysis : an Official Publication of the Society for Risk Analysis|February 24, 2017
Sizing Up a Superstorm: Exploring the Role of Recalled Experience and Attribution of Responsibility in Judgments of Future Hurricane RiskLaura N Rickard, Z Janet Yang, Jonathon P Schuldt, et al.
Forschende Komplementarmedizin Und Klassische Naturheilkunde = Research in Complementary and Natural Classical Medicine|July 11, 2003
Pretreatment with thyroxine (10-(8) parts by weight) enhances a 'curative' effect of homeopathically prepared thyroxine (10-(13)) on lowland frogsP C Endler, R Lüdtke, C Heckmann, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridizationS W Scherer, H H Heng, G W Robinson, et al.
Nature Genetics|November 1, 1996
Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Pageof 92

Showing results (351-360 of 915) with videos related to

Sort By:
Pageof 92
Molecular Genetics & Genomic Medicine|October 20, 2021
Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testingIskra Peltekova, Afiqah Yusuf, Jennifer Frei, et al.
Journal of Genetic Counseling|September 7, 2020
Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditionsAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
BMC Medical Genetics|May 8, 2020
Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerAnna Bobyn, Mehdi Zarrei, Yuankun Zhu, et al.
Respiration Physiology|March 1, 1993
Microemboli reduce phase III slopes of CO2 and invert phase III slopes of infused SF6M S Schreiner, L G Leksell, S R Gobran, et al.
Blood|May 1, 1996
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasiaE J Johnson, S W Scherer, L Osborne, et al.
Diabetes|March 29, 2005
Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics StudyAndrew P Boright, Andrew D Paterson, Lucia Mirea, et al.
Risk Analysis : an Official Publication of the Society for Risk Analysis|February 24, 2017
Sizing Up a Superstorm: Exploring the Role of Recalled Experience and Attribution of Responsibility in Judgments of Future Hurricane RiskLaura N Rickard, Z Janet Yang, Jonathon P Schuldt, et al.
Forschende Komplementarmedizin Und Klassische Naturheilkunde = Research in Complementary and Natural Classical Medicine|July 11, 2003
Pretreatment with thyroxine (10-(8) parts by weight) enhances a 'curative' effect of homeopathically prepared thyroxine (10-(13)) on lowland frogsP C Endler, R Lüdtke, C Heckmann, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridizationS W Scherer, H H Heng, G W Robinson, et al.
Nature Genetics|November 1, 1996
Mutations in the human Sonic Hedgehog gene cause holoprosencephalyE Roessler, E Belloni, K Gaudenz, et al.
Pageof 92