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American Journal of Human Genetics|June 1, 1995
New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndromeM Jouet, A Moncla, J Paterson, et al.
American Journal of Medical Genetics|June 28, 1996
Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotypeB E Ahlbom, P Goetz, J R Korenberg, et al.
American Journal of Human Genetics|June 1, 1993
Linkage mapping of a severe X-linked mental retardation syndromeH Malmgren, M Sundvall, N Dahl, et al.
The Pharmacogenomics Journal|December 17, 2003
Warfarin sensitivity related to CYP2C9, CYP3A5, ABCB1 (MDR1) and other factorsM Wadelius, K Sörlin, O Wallerman, et al.
Clinical Genetics|September 1, 1992
The gene for Best's macular dystrophy is located at 11q13 in a Swedish familyK Forsman, C Graff, S Nordström, et al.
Genome Research|December 1, 1996
Chromosome-specific panels of tri- and tetranucleotide microsatellite markers for multiplex fluorescent detection and automated genotyping: evaluation of their utility in pathology and forensicsA K Lindqvist, P K Magnusson, J Balciuniene, et al.
Human Genetics|June 1, 1989
Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndromeN Dahl, K Hammarström-Heeroma, P Goonewardena, et al.
Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.
The Pharmacogenomics Journal|May 11, 2005
Common VKORC1 and GGCX polymorphisms associated with warfarin doseM Wadelius, L Y Chen, K Downes, et al.
Pharmacogenetics|September 2, 1999
Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancerM Wadelius, J L Autrup, M J Stubbins, et al.
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