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Molecular mapping of alzheimer-type dementia in Down's syndrome

Annals of neurology, 1998-03, Vol.43 (3), p.380-383

1998

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MTHFR association with arteriosclerotic vascular disease?

Human genetics, 1998-07, Vol.103 (1), p.11-21

1998

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Association of the TNF-α-308 (G→A) polymorphism with self-reported history of childhood asthma

Human genetics, 2000-12, Vol.107 (6), p.591-596

2000

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Expression of the developmental and oncogenic PAX2 gene in human prostate cancer

The Journal of urology, 2001-06, Vol.165 (6 Pt 1), p.2115

2001

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Mortality in Women with Turner Syndrome in Great Britain: A National Cohort Study

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4735-4742

2008

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Maternal leptin receptor gene variant Gln223Arg is not associated with variation in birth weight or maternal body mass index in UK and South Asian populations

International Journal of Obesity, 2001-05, Vol.25 (5), p.753-755

2001

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The expression of PAX5 in human transitional cell carcinoma of the bladder: relationship with de‐differentiation

BJU international, 1999-06, Vol.83 (9), p.1039-1044

1999

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Purification, properties, and diagnosis of banana bract mosaic potyvirus and its distinction from abaca mosaic potyvirus

Phytopathology, 1997-07, Vol.87 (7), p.698-705

1997

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Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health

American journal of epidemiology, 1999-12, Vol.150 (11), p.1229-1237

1999

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Survivin gene expression and prognosis in recurrent colorectal cancer

Gut, 2001-01, Vol.48 (1), p.137-138

2001

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Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Human genetics, 2000-11, Vol.107 (5), p.476-482

2000

Volltextzugriff (PDF)

Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-receptor gene defect

Atherosclerosis, 1996-01, Vol.119 (1), p.43-55

1996

Volltextzugriff (PDF)

Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent

Journal of lipid research, 1995-01, Vol.36 (1), p.117-124

1995

Volltextzugriff (PDF)

Novel Methodology for the Detection of Chromosome 21-Specific α-Satellite DNA Sequences

Genomics (San Diego, Calif.), 1999-05, Vol.57 (3), p.429-432

1999

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Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome

Neuroreport, 1997-05, Vol.8 (7), p.1645-1649

1997

Volltextzugriff (PDF)

Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome)

Annals of human genetics, 1995-07, Vol.59 (3), p.253-269

1995

Volltextzugriff (PDF)

Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health

Arteriosclerosis and thrombosis, 1991-07, Vol.11 (4), p.1100

1991

Volltextzugriff (PDF)

Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2

Mammalian genome, 1997-05, Vol.8 (5), p.342-345

1997

Volltextzugriff (PDF)

Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians

Human genetics, 1992-03, Vol.88 (5), p.529-536

1992

Volltextzugriff (PDF)

Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Human genetics, 2000-05, Vol.106 (5), p.525-530

2000

Volltextzugriff (PDF)

Genetic initiation, progression and prognostic markers in transitional cell carcinoma of the bladder: a summary of the structural and transcriptional changes, and the role of developmental genes

British Journal of Urology, 1998-10, Vol.82 (4), p.503-512

1998

Volltextzugriff (PDF)

Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster

American journal of human genetics, 1991-08, Vol.49 (2), p.350-365

1991

Volltextzugriff (PDF)

Genetic Structure and the Search for Genotype-Phenotype Relationships: An Example from Disequilibrium in the Apo B Gene Region

Genetics (Austin), 1991-10, Vol.129 (2), p.525-533

1991

Volltextzugriff (PDF)

Conserved gene sequences for species identification : PCR analysis of the 3' UTR of the SON gene distinguishes human and other mammalian DNAs

Forensic science international, 1995-06, Vol.73 (3), p.171-181

1995

Volltextzugriff (PDF)

A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations

Genetics (Austin), 1988-12, Vol.120 (4), p.1145-1154

1988

Volltextzugriff (PDF)

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Molecular mapping of alzheimer-type dementia in Down's syndrome

MTHFR association with arteriosclerotic vascular disease?

Association of the TNF-α-308 (G→A) polymorphism with self-reported history of childhood asthma

Expression of the developmental and oncogenic PAX2 gene in human prostate cancer

Mortality in Women with Turner Syndrome in Great Britain: A National Cohort Study

Maternal leptin receptor gene variant Gln223Arg is not associated with variation in birth weight or maternal body mass index in UK and South Asian populations

The expression of PAX5 in human transitional cell carcinoma of the bladder: relationship with de‐differentiation

Purification, properties, and diagnosis of banana bract mosaic potyvirus and its distinction from abaca mosaic potyvirus

Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health

Survivin gene expression and prognosis in recurrent colorectal cancer

Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-receptor gene defect

Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent

Novel Methodology for the Detection of Chromosome 21-Specific α-Satellite DNA Sequences

Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome

Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome)

Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health

Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2

Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians

Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Genetic initiation, progression and prognostic markers in transitional cell carcinoma of the bladder: a summary of the structural and transcriptional changes, and the role of developmental genes

Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster

Genetic Structure and the Search for Genotype-Phenotype Relationships: An Example from Disequilibrium in the Apo B Gene Region

Conserved gene sequences for species identification : PCR analysis of the 3' UTR of the SON gene distinguishes human and other mammalian DNAs

A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations

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