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C B Whitley

Showing results (51-60 of 58) with videos related to

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International Journal of Pediatric Otorhinolaryngology|February 1, 1988
Resolution of obstructive sleep apnea in Hurler syndrome after bone marrow transplantationB N Malone, C B Whitley, A J Duvall, et al.
American Journal of Medical Genetics|October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathologyC B Whitley, L O Langer, J Ophoven, et al.
Bone Marrow Transplantation|December 20, 2011
Increased longevity and metabolic correction following syngeneic BMT in a murine model of mucopolysaccharidosis type ID A Wolf, A W Lenander, Z Nan, et al.
American Journal of Medical Genetics|April 15, 1993
Long-term outcome of Hurler syndrome following bone marrow transplantationC B Whitley, K G Belani, P N Chang, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Persistent succinylacetone excretion after liver transplantation in a patient with hereditary tyrosinaemia type IM Tuchman, D K Freese, H L Sharp, et al.
American Journal of Human Genetics|March 7, 1998
NAGLU mutations underlying Sanfilippo syndrome type BA Schmidtchen, D Greenberg, H G Zhao, et al.
Birth Defects Original Article Series|January 1, 1986
Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantationB R Blazar, C B Whitley, R J Desnick, et al.
Human Gene Therapy|March 1, 1996
Retroviral-mediated transfer of the iduronate-2-sulfatase gene into lymphocytes for treatment of mild Hunter syndrome (mucopolysaccharidosis type II)C B Whitley, R S McIvor, E L Aronovich, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
International Journal of Pediatric Otorhinolaryngology|February 1, 1988
Resolution of obstructive sleep apnea in Hurler syndrome after bone marrow transplantationB N Malone, C B Whitley, A J Duvall, et al.
American Journal of Medical Genetics|October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathologyC B Whitley, L O Langer, J Ophoven, et al.
Bone Marrow Transplantation|December 20, 2011
Increased longevity and metabolic correction following syngeneic BMT in a murine model of mucopolysaccharidosis type ID A Wolf, A W Lenander, Z Nan, et al.
American Journal of Medical Genetics|April 15, 1993
Long-term outcome of Hurler syndrome following bone marrow transplantationC B Whitley, K G Belani, P N Chang, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Persistent succinylacetone excretion after liver transplantation in a patient with hereditary tyrosinaemia type IM Tuchman, D K Freese, H L Sharp, et al.
American Journal of Human Genetics|March 7, 1998
NAGLU mutations underlying Sanfilippo syndrome type BA Schmidtchen, D Greenberg, H G Zhao, et al.
Birth Defects Original Article Series|January 1, 1986
Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantationB R Blazar, C B Whitley, R J Desnick, et al.
Human Gene Therapy|March 1, 1996
Retroviral-mediated transfer of the iduronate-2-sulfatase gene into lymphocytes for treatment of mild Hunter syndrome (mucopolysaccharidosis type II)C B Whitley, R S McIvor, E L Aronovich, et al.
Pageof 6