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C B Whitley

Showing results (11-20 of 58) with videos related to

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American Journal of Human Genetics|March 7, 1998
Genotype-phenotype correspondence in Sanfilippo syndrome type BH G Zhao, E L Aronovich, C B Whitley
Neuropediatrics|April 1, 1992
Heterozygosity for the "DN allele" (G533-greater than A) of the beta-hexosaminidase alpha subunit gene identified by direct DNA sequencing in a family with the B1 variant of GM2-gangliosidosisC B Whitley, R A Anderson, R S McIvor
Blood|April 15, 1990
Busulfan disposition in childrenL B Grochow, W Krivit, C B Whitley, et al.
Gene Therapy|December 8, 2000
Retroviral vector design studies toward hematopoietic stem cell gene therapy for mucopolysaccharidosis type ID Pan, E Aronovich, R S McIvor, et al.
Human Gene Therapy|December 10, 1999
Combined ultrafiltration-transduction in a hollow-fiber bioreactor facilitates retrovirus-mediated gene transfer into peripheral blood lymphocytes from patients with mucopolysaccharidosis type IID Pan, R Shankar, D F Stroncek, et al.
Pediatric Radiology|September 12, 1997
Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): imaging findings following bone marrow transplantationS H Hite, W Krivit, S J Haines, et al.
American Journal of Medical Genetics|September 1, 1986
de la Chapelle dysplasiaC B Whitley, B A Burke, G Granroth, et al.
Journal of Hematotherapy|January 27, 1999
Mobilization and transduction of peripheral blood progenitor cells in patients with mucopolysaccharidosis IA Hubel, D Stroncek, D Pan, et al.
Birth Defects Original Article Series|January 1, 1986
Bone marrow transplantation for Hurler syndrome: assessment of metabolic correctionC B Whitley, N K Ramsay, J H Kersey, et al.
Human Gene Therapy|September 25, 1999
Enzymatic correction and cross-correction of mucopolysaccharidosis type I fibroblasts by adeno-associated virus-mediated transduction of the alpha-L-iduronidase geneS D Hartung, R G Reddy, C B Whitley, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|March 7, 1998
Genotype-phenotype correspondence in Sanfilippo syndrome type BH G Zhao, E L Aronovich, C B Whitley
Neuropediatrics|April 1, 1992
Heterozygosity for the "DN allele" (G533-greater than A) of the beta-hexosaminidase alpha subunit gene identified by direct DNA sequencing in a family with the B1 variant of GM2-gangliosidosisC B Whitley, R A Anderson, R S McIvor
Blood|April 15, 1990
Busulfan disposition in childrenL B Grochow, W Krivit, C B Whitley, et al.
Gene Therapy|December 8, 2000
Retroviral vector design studies toward hematopoietic stem cell gene therapy for mucopolysaccharidosis type ID Pan, E Aronovich, R S McIvor, et al.
Human Gene Therapy|December 10, 1999
Combined ultrafiltration-transduction in a hollow-fiber bioreactor facilitates retrovirus-mediated gene transfer into peripheral blood lymphocytes from patients with mucopolysaccharidosis type IID Pan, R Shankar, D F Stroncek, et al.
Pediatric Radiology|September 12, 1997
Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): imaging findings following bone marrow transplantationS H Hite, W Krivit, S J Haines, et al.
American Journal of Medical Genetics|September 1, 1986
de la Chapelle dysplasiaC B Whitley, B A Burke, G Granroth, et al.
Journal of Hematotherapy|January 27, 1999
Mobilization and transduction of peripheral blood progenitor cells in patients with mucopolysaccharidosis IA Hubel, D Stroncek, D Pan, et al.
Birth Defects Original Article Series|January 1, 1986
Bone marrow transplantation for Hurler syndrome: assessment of metabolic correctionC B Whitley, N K Ramsay, J H Kersey, et al.
Human Gene Therapy|September 25, 1999
Enzymatic correction and cross-correction of mucopolysaccharidosis type I fibroblasts by adeno-associated virus-mediated transduction of the alpha-L-iduronidase geneS D Hartung, R G Reddy, C B Whitley, et al.
Pageof 6