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Biochemical Medicine and Metabolic Biology|December 1, 1986
Elevation of urinary hyaluronic acid in Werner's syndrome and progeriaF J Kieras, W T Brown, G E Houck, et al.
Biochemical Medicine|April 1, 1984
Low sulfated glycosaminoglycans are excreted in patients with the Lowe syndromeF J Kieras, G E Houck, J H French, et al.
American Journal of Medical Genetics|July 15, 1994
Mosaicism in fragile X affected malesS L Nolin, A Glicksman, G E Houck, et al.
Annals of Neurology|July 1, 1984
Ultrastructural, neurological, and glycosaminoglycan abnormalities in lowe's syndromeK E Wisniewski, F J Kieras, J H French, et al.
American Journal of Human Genetics|January 1, 1985
Chromosomal localization of several families of repetitive sequences by in situ hybridizationE A Devine, S L Nolin, G E Houck, et al.
American Journal of Medical Genetics|July 15, 1994
Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese populationN Zhong, X Liu, S Gou, et al.
American Journal of Human Genetics|August 12, 1999
FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation malesS L Nolin, G E Houck, A D Gargano, et al.
Biochemical and Biophysical Research Communications|May 31, 1984
Isolation and regional localization by in situ hybridization of a unique gene segment to chromosome 21E A Devine, S L Nolin, G E Houck, et al.
American Journal of Medical Genetics|August 9, 1996
Reverse mutations in the fragile X syndromeW T Brown, G E Houck, X Ding, et al.
Neuropediatrics|May 1, 1985
Sanfilippo disease, type A with some features of ceroid lipofuscinosisK Wisniewski, R Rudelli, M Laure-Kamionowska, et al.
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