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Clinical Genetics|November 18, 2003
Genetic variation in the promoter and 5' UTR of the copper transporter, ATP7B, in patients with Wilson diseaseL M Cullen, L Prat, D W Cox
American Journal of Human Genetics|June 19, 1998
The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populationsL M Cullen, X Gao, S Easteal, et al.
Gastroenterology|May 30, 1998
Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutationD H Crawford, E C Jazwinska, L M Cullen, et al.
Annual Review of Medicine|March 12, 1999
Genetics of hemochromatosisL M Cullen, G J Anderson, G A Ramm, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1997
Isolation and characterisation of cosmids to intervals within a 4.5Mb region at 6p21.3E C Jazwinska, L M Cullen, A Zournazi, et al.
Human Genetics|April 1, 1994
Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defectsG E Davies, C M Howard, M J Farrer, et al.
American Journal of Human Genetics|March 31, 2000
Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twinsJ B Whitfield, L M Cullen, E C Jazwinska, et al.
American Journal of Human Genetics|August 1, 1993
Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defectC M Howard, G E Davies, M J Farrer, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Generation of a transcription map distal to HLA-FS Goldwurm, B F Van der Griend, J L Banyer, et al.
Annals of Human Genetics|July 1, 1995
Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome)G E Davies, C M Howard, M J Farrer, et al.
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