Whitley CB, Draper KM, Dutton CM, Brown PA, Severson SL, France LA: Diagnostic test for 
mucopolysaccharidosis. H Rapid quantification of glycosaminoglycan in urine samples collected on 
paper matrix. Clin Chem 35:2074-2081, 1989. 
Krivit W, Whitley CB, Chang PN, Shapiro E, Belani KG, Summers CG, Blazar B. Lysosomal storage 
diseases treated by bone marrow transplantation: review of 21 patients. In: Bone Marrow 
Transplantation in Children (Eds: Johnson FL, Pochedly C), Raven Press, Ltd: New York, 1990. 
Whitley CB, Gorlin RJ. Adams-Oliver syndrome revisited. Am J Med Genet 40: 319-326, 1991 
Whitley CB, Anderson RA, Mclvor RS. Heterozygosity for the DN allele (G 533 ->A) of the 6- 
hexosaminidase a subunit gene idenufied by direct DNA sequencing in a family with the B1 variant of 
GM 2 -g an gliosidosis. Neuropediatrics 23:96-101, 1992. 
Braunlin EA, Hunter DW, Krivit W, Burke BA, Hesslein PS, Porter PT, Whitley CB. Evaluation of coronary 
artery disease in the Hurler syndrome by angiography. Am J Cardiol 69:1487-1492, 1992. 
Crotty PL, Braun SE, Anderson RA, Whitley CB: Mutation R468W of the iduronate-2-sulfatase gene in mild 
Hunter syndrome (mucopolysaccharidosis type II) confirmed by in vitro mutagenesis and expression. 
Hum Mol Genet 1:755-757, 1992. 
Resnick JM, Krivit W, Snover DC, Kersey JH, Ramsay NKC, Blazar BR, Whitley CB. Pathology of the 
liver in mucopolysaccharidoses: light and electron microscopic assessment before and after bone marrow 
transplantation. Bone Marrow Transplantation 10:273-280, 1992. 
Crotty PL, Whitley CB. Assessment of iduronate-2-sulfatase mRNA expression in Hunter syndrome 
(mucopolysaccharidosis type II), Hum Genet 90:285-288, 1992. 
Belani KG, Krivit W, Carpenter BLM, Braunlin E, Liao J-C, Floyd T, Leonard AS, Summers CG, Levine S, 
Whitley CB. Children with mucopolysaccharidosis: perioperative care, morbidity, mortality, and new 
findings. J Pediatr Surg, 28:403-410, 1993. 
Whitley CB, Belani K, Chang PN, Summers CG, Blazar BR, Tsai MY, Latchaw RE, Ramsay NKC, Kersey 
JH: Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet 
46:209-218, 1993. 
Whitley CB, Anderson RA, Crotty PL, Anyane-Yeboa K, Russo D, Warburton DW: Caveat to genotype- 
phenotype correlation: discordant clinical severity of R468W and R468Q mutations of the iduronate-2- 
sulfatase gene, Hum Mutation 2:235-237, 1993. 
Whitley CB, The mucopolysaccharidoses. In: Beighton P (ed), McKusick's Heritable Diseases of Connective 
Tissue, 5th ed, 1993, pp. 367-499. 
Braun SE, Anderson RA, Crotty PL, Mclvor RS, Whitley CB: Correction of mucopolysaccharidosis type II 
(Hunter syndrome) by retroviral-mediated gene transfer and expression of human iduronate-2-sulfatase in 
lymphoblastoid cell lines. Proc Natl Acad Sci USA 90:1830-11834, 1993. 
Resnick JM, Whitley CB, Leonard AS, Krivit W, Snover DC: Light and electron microscopic features of the 
liver in mucopolysaccharidosis, Hum Pathol 25:276-286, 1994. 
Summers CG, Whitley CB, Holland EJ, Purple RL, Krivit W: Dense peripheral corneal clouding in Scheie 
syndrome, Cornea, in press. 
Klein KA, Krivit W, Whitley CB, Peters C, de Alarcon P, Cool VA, Klemperer M, Miller L, Nelson RP, 
Henslee-Downey J, Fuhrman M, Chang P-N, Lockman L, Shapiro EG: Poor cognitive outcome of 
eleven children with Sanfilippo syndrome after bone marrow transplantation and successful engraftment. 
Bone Marrow Transplantation, in press. 
Jonsson JJ, Aronovich EL, Braun, SE, Whitley CB: Molecular diagnosis of mucopolysaccharidosis type II 
(Hunter syndrome) by automated sequencing of the coding region and computer-assisted analysis: toward 
mapping of mutations in the iduronate-2-sulfatase gene, submitted for publication. 
Braun SE, Jonsson JJ, Aronovich EL, Mclvor RS, Whitley CB: A model of ex vivo lymphocyte gene 
therapy for Hunter syndrome, mucopolysaccharidosis type n, in preparation. 
Whitley CB, Ramsay NKC, Kersey JH, Chang PN, Latchaw RE, Blazar BR, Scott HS, Nelson PV, Morris 
CP, Hop wood JJ: Mutation analysis and clinical outcome of patients with Hurler syndrome 
(mucopolysaccharidosis type I-H) undergoing bone marrow transplantation, in preparation. 
Pan D, Braun SE, Jonsson JJ, Aronovich EL, Mclvor RS, Whitley CB: In vitro correction of iduronate-2- 
sulfatase deficiency in Hunter syndrome (mucopolysaccharidosis type II) with four retroviral vectors, in 
preparation. 
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