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Anna Erlandson

Showing results (1-10 of 7) with videos related to

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Journal of Child Neurology|October 18, 2005
MECP2 abnormality phenotypes: clinicopathologic area with broad variabilityAnna Erlandson, Bengt Hagberg
Molecular Medicine Reports|April 12, 2011
Epigenetic mutations in CDKN2A in western Swedish families with hereditary malignant melanomaAnna Erlandson, Frida Appelqvist, Charlotta Enerbäck
Acta Paediatrica (Oslo, Norway : 1992)|July 20, 2011
Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old childrenMikael Lundvall, Saideh Rajaei, Anna Erlandson, et al.
Genes, Chromosomes & Cancer|May 8, 2014
Deletion of the MGMT gene in familial melanomaFrida Appelqvist, Maria Yhr, Anna Erlandson, et al.
The Journal of Investigative Dermatology|January 27, 2007
Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanomaAnna Erlandson, Frida Appelqvist, Ann-Marie Wennberg, et al.
Genetic Testing|March 6, 2004
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patientsAnna Erlandson, Lena Samuelsson, Bengt Hagberg, et al.
Journal of Child Neurology|January 8, 2011
Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysisSaideh Rajaei, Anna Erlandson, Marten Kyllerman, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Child Neurology|October 18, 2005
MECP2 abnormality phenotypes: clinicopathologic area with broad variabilityAnna Erlandson, Bengt Hagberg
Molecular Medicine Reports|April 12, 2011
Epigenetic mutations in CDKN2A in western Swedish families with hereditary malignant melanomaAnna Erlandson, Frida Appelqvist, Charlotta Enerbäck
Acta Paediatrica (Oslo, Norway : 1992)|July 20, 2011
Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old childrenMikael Lundvall, Saideh Rajaei, Anna Erlandson, et al.
Genes, Chromosomes & Cancer|May 8, 2014
Deletion of the MGMT gene in familial melanomaFrida Appelqvist, Maria Yhr, Anna Erlandson, et al.
The Journal of Investigative Dermatology|January 27, 2007
Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanomaAnna Erlandson, Frida Appelqvist, Ann-Marie Wennberg, et al.
Genetic Testing|March 6, 2004
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patientsAnna Erlandson, Lena Samuelsson, Bengt Hagberg, et al.
Journal of Child Neurology|January 8, 2011
Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysisSaideh Rajaei, Anna Erlandson, Marten Kyllerman, et al.
Pageof 1