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R P Erickson

Showing results (341-350 of 347) with videos related to

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Genomics|December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17S R Diehl, M Boehnke, R P Erickson, et al.
Science (New York, N.Y.)|July 7, 1995
Regulation of human gene therapyG A Chase, P A DeLeon, K R Dronamraju, et al.
American Journal of Human Genetics|January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.
Molecular Psychiatry|July 20, 2005
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistanceH A Garriock, J J B Allen, P Delgado, et al.
Lymphology|November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutationD J Mustacich, R I Kylat, M J Bernas, et al.
Journal of Medical Genetics|November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsR P Erickson, S L Dagenais, M S Caulder, et al.
Journal of Medical Genetics|December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de LangeJ Yan, F Zhang, E Brundage, et al.
Pageof 35

Showing results (341-350 of 347) with videos related to

Sort By:
Pageof 35
You have reached the last page of results.This site can display upto 347 results.
Genomics|December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17S R Diehl, M Boehnke, R P Erickson, et al.
Science (New York, N.Y.)|July 7, 1995
Regulation of human gene therapyG A Chase, P A DeLeon, K R Dronamraju, et al.
American Journal of Human Genetics|January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.
Molecular Psychiatry|July 20, 2005
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistanceH A Garriock, J J B Allen, P Delgado, et al.
Lymphology|November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutationD J Mustacich, R I Kylat, M J Bernas, et al.
Journal of Medical Genetics|November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsR P Erickson, S L Dagenais, M S Caulder, et al.
Journal of Medical Genetics|December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de LangeJ Yan, F Zhang, E Brundage, et al.
Pageof 35