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Journal of Hepatology|March 1, 1990
Polymerase chain reaction for detection of the alpha-1-antitrypsin Z allele in chronic liver diseaseA M Brind, I McIntosh, D J Brock, et al.American Journal of Human Genetics|July 1, 1993
Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.Genomics|July 1, 1996
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16M H Polymeropoulos, S E Ide, M Wright, et al.Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.JAMA|September 18, 1996
Career development for women in academic medicine: Multiple interventions in a department of medicineL P Fried, C A Francomano, S M MacDonald, et al.Journal of Medical Genetics|February 1, 1990
An exclusion map of Marfan syndromeS H Blanton, M Sarfarazi, H Eiberg, et al.The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.The Journal of Biological Chemistry|March 21, 1998
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutationM A Weis, D J Wilkin, H J Kim, et al.American Journal of Human Genetics|October 30, 1998
A second locus for familial high myopia maps to chromosome 12qT L Young, S M Ronan, A B Alvear, et al.Pageof 17