O Parolini|M E Conley - JoVE Visualize

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Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994

X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and pubertyF Buzi, L D Notarangelo, A Plebani, et al.

Journal of Materials Science. Materials in Medicine|December 17, 2009

Ability of polyurethane foams to support placenta-derived cell adhesion and osteogenic differentiation: preliminary resultsS Bertoldi, S Farè, M Denegri, et al.

The Journal of Pediatrics|July 1, 1996

Wiskott-Aldrich syndrome in a family with Fanconi anemiaJ Rohrer, R C Ribeiro, A D Auerbach, et al.

Clinical Genetics|January 26, 2007

A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WASA K Dobbs, T Yang, D M Farmer, et al.

Journal of Tissue Engineering and Regenerative Medicine|September 29, 2011

Characterization and potential applications of progenitor-like cells isolated from horse amniotic membraneA Lange-Consiglio, B Corradetti, D Bizzaro, et al.

Life Sciences|January 1, 1997

A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficienciesG S Wengler, O Parolini, M Fiorini, et al.

Journal of Pediatric Gastroenterology and Nutrition|May 1, 1988

Multifocal adenocarcinoma of the stomach in a child with common variable immunodeficiencyM E Conley, M M Ziegler, S Borden, et al.

The Journal of Clinical Investigation|October 19, 1999

Mutations in Igalpha (CD79a) result in a complete block in B-cell developmentY Minegishi, E Coustan-Smith, L Rapalus, et al.

AJNR. American Journal of Neuroradiology|April 14, 2006

Diffuse CNS vasculopathy with chronic Epstein-Barr virus infection in X-linked lymphoproliferative diseaseJ K Weeks, K J Helton, M E Conley, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 1, 1988

Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiencyM E Conley, A Lavoie, C Briggs, et al.

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Showing results (61-70 of 118) with videos related to

Sort By:

Pageof 12

Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994

X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and pubertyF Buzi, L D Notarangelo, A Plebani, et al.

Journal of Materials Science. Materials in Medicine|December 17, 2009

Ability of polyurethane foams to support placenta-derived cell adhesion and osteogenic differentiation: preliminary resultsS Bertoldi, S Farè, M Denegri, et al.

The Journal of Pediatrics|July 1, 1996

Wiskott-Aldrich syndrome in a family with Fanconi anemiaJ Rohrer, R C Ribeiro, A D Auerbach, et al.

Clinical Genetics|January 26, 2007

A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WASA K Dobbs, T Yang, D M Farmer, et al.

Journal of Tissue Engineering and Regenerative Medicine|September 29, 2011

Characterization and potential applications of progenitor-like cells isolated from horse amniotic membraneA Lange-Consiglio, B Corradetti, D Bizzaro, et al.

Life Sciences|January 1, 1997

A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficienciesG S Wengler, O Parolini, M Fiorini, et al.

Journal of Pediatric Gastroenterology and Nutrition|May 1, 1988

Multifocal adenocarcinoma of the stomach in a child with common variable immunodeficiencyM E Conley, M M Ziegler, S Borden, et al.

The Journal of Clinical Investigation|October 19, 1999

Mutations in Igalpha (CD79a) result in a complete block in B-cell developmentY Minegishi, E Coustan-Smith, L Rapalus, et al.

AJNR. American Journal of Neuroradiology|April 14, 2006

Diffuse CNS vasculopathy with chronic Epstein-Barr virus infection in X-linked lymphoproliferative diseaseJ K Weeks, K J Helton, M E Conley, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 1, 1988

Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiencyM E Conley, A Lavoie, C Briggs, et al.

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