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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1988
Transfusion of carbonic anhydrase-replete erythrocytes fails to correct the acidification defect in the syndrome of osteopetrosis, renal tubular acidosis, and cerebral calcification (carbonic anhydrase-II deficiency)M P Whyte, L L Hamm, W S SlyThe Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Hepatitis C-associated osteosclerosis: late onset after blood transfusion in an elderly womanJ L Shaker, W R Reinus, M P WhyteBone|January 16, 1998
X-linked hypophosphatemia: normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-induced renal azotemiaM C Eddy, W H McAlister, M P WhyteRadiology|February 1, 1987
Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic ricketsW H McAlister, G S Kim, M P WhyteSkeletal Radiology|January 1, 1986
Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive conditionW H McAlister, J D Coe, M P WhyteGenomics|September 23, 1997
Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEXM Grieff, M P Whyte, R V Thakker, et al.Pediatric Research|October 1, 1985
Positive renal response to intravenous acetazolamide in patients with carbonic anhydrase II deficiencyW S Sly, M P Whyte, T Krupin, et al.American Journal of Medical Genetics|October 6, 1999
Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not brokenR M Pauli, P Modaff, S L Sipes, et al.Gene|October 12, 2001
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice siteS Mumm, X Zhang, M Vacca, et al.The Journal of Pediatrics|July 1, 1991
Hypercalciuria in children severely affected with osteogenesis imperfectaA Chines, D J Petersen, F W Schranck, et al.Pageof 16