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Anne Maddalena

Showing results (1-10 of 6) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2005
Technical standards and guidelines: molecular genetic testing for ultra-rare disordersAnne Maddalena, Sherri Bale, Soma Das, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2002
Standards and guidelines for CFTR mutation testingCarolyn Sue Richards, Linda A Bradley, Jean Amos, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation|December 3, 2009
Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)Marcus Gentsch, Aneta Kaczmarczyk, Karin van Leeuwen, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2005
Technical standards and guidelines: molecular genetic testing for ultra-rare disordersAnne Maddalena, Sherri Bale, Soma Das, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2002
Standards and guidelines for CFTR mutation testingCarolyn Sue Richards, Linda A Bradley, Jean Amos, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation|December 3, 2009
Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)Marcus Gentsch, Aneta Kaczmarczyk, Karin van Leeuwen, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Pageof 1