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B K Goodman

Showing results (11-20 of 27) with videos related to

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Cancer Genetics and Cytogenetics|September 24, 2004
A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12C A Tirado, J Lager, P M Rosoff, et al.
Somatic Cell and Molecular Genetics|November 1, 1996
Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapyP B Wissmann, B K Goodman, J G Vockley, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)patB K Goodman, K Stone, J M Coddett, et al.
Genomics|April 25, 2000
Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES)V Praphanphoj, B K Goodman, G H Thomas, et al.
Cancer Genetics and Cytogenetics|July 30, 2003
Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21)C A Tirado, V Golembiewski-Ruiz, J Horvatinovich, et al.
Neurology|April 6, 2000
Quantitative neurologic assessment of ataxia-telangiectasiaT O Crawford, A S Mandir, M A Lefton-Greif, et al.
Biochemical and Molecular Medicine|October 1, 1996
Loss of function mutations in conserved regions of the human arginase I geneJ G Vockley, B K Goodman, D E Tabor, et al.
American Journal of Medical Genetics|September 5, 1997
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden diseaseE M Arch, B K Goodman, R A Van Wesep, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
Human Mutation|January 1, 1994
Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemiaJ G Vockley, D E Tabor, R M Kern, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|September 24, 2004
A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12C A Tirado, J Lager, P M Rosoff, et al.
Somatic Cell and Molecular Genetics|November 1, 1996
Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapyP B Wissmann, B K Goodman, J G Vockley, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)patB K Goodman, K Stone, J M Coddett, et al.
Genomics|April 25, 2000
Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES)V Praphanphoj, B K Goodman, G H Thomas, et al.
Cancer Genetics and Cytogenetics|July 30, 2003
Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21)C A Tirado, V Golembiewski-Ruiz, J Horvatinovich, et al.
Neurology|April 6, 2000
Quantitative neurologic assessment of ataxia-telangiectasiaT O Crawford, A S Mandir, M A Lefton-Greif, et al.
Biochemical and Molecular Medicine|October 1, 1996
Loss of function mutations in conserved regions of the human arginase I geneJ G Vockley, B K Goodman, D E Tabor, et al.
American Journal of Medical Genetics|September 5, 1997
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden diseaseE M Arch, B K Goodman, R A Van Wesep, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
Human Mutation|January 1, 1994
Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemiaJ G Vockley, D E Tabor, R M Kern, et al.
Pageof 3