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B K Goodman

Showing results (21-30 of 27) with videos related to

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American Journal of Human Genetics|April 25, 2000
Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemiaK A Sacksteder, B J Biery, J C Morrell, et al.
Nature Genetics|June 16, 1999
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporterJ A Camacho, C Obie, B Biery, et al.
American Journal of Medical Genetics|June 22, 2000
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12)C B Cargile, I McIntosh, M V Clough, et al.
Leukemia|December 1, 2009
Single-cell analysis reveals oligoclonality among 'low-count' monoclonal B-cell lymphocytosisM C Lanasa, S D Allgood, A D Volkheimer, et al.
American Journal of Human Genetics|June 1, 1992
Molecular genetic study of human arginase deficiencyW W Grody, D Klein, A E Dodson, et al.
American Journal of Medical Genetics|December 18, 1998
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated familiesB K Goodman, L G Shaffer, J Rutberg, et al.
Leukemia|May 28, 2011
Immunophenotypic and gene expression analysis of monoclonal B-cell lymphocytosis shows biologic characteristics associated with good prognosis CLLM C Lanasa, S D Allgood, S L Slager, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
American Journal of Human Genetics|April 25, 2000
Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemiaK A Sacksteder, B J Biery, J C Morrell, et al.
Nature Genetics|June 16, 1999
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporterJ A Camacho, C Obie, B Biery, et al.
American Journal of Medical Genetics|June 22, 2000
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12)C B Cargile, I McIntosh, M V Clough, et al.
Leukemia|December 1, 2009
Single-cell analysis reveals oligoclonality among 'low-count' monoclonal B-cell lymphocytosisM C Lanasa, S D Allgood, A D Volkheimer, et al.
American Journal of Human Genetics|June 1, 1992
Molecular genetic study of human arginase deficiencyW W Grody, D Klein, A E Dodson, et al.
American Journal of Medical Genetics|December 18, 1998
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated familiesB K Goodman, L G Shaffer, J Rutberg, et al.
Leukemia|May 28, 2011
Immunophenotypic and gene expression analysis of monoclonal B-cell lymphocytosis shows biologic characteristics associated with good prognosis CLLM C Lanasa, S D Allgood, S L Slager, et al.
Pageof 3