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DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys

Proceedings of the Royal Society. B, Biological sciences, 1999-05, Vol.266 (1422), p.901-904

1999

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Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

Nature genetics, 1997-12, Vol.17 (4), p.449-452

1997

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Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

Electrophoresis, 1998-12, Vol.19 (18), p.3055-3061

1998

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Telomeric lengths and telomerase activity in liposarcomas

Molecular carcinogenesis, 1999-02, Vol.24 (2), p.144-151

1999

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Friedreich's ataxia: Revision of the phenotype according to molecular genetics

Brain (London, England : 1878), 1997-12, Vol.120 (12), p.2131-2140

1997

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Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14, and Y in various Eurasian populations

Human genetics, 1994-05, Vol.93 (5), p.592-596

1994

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Males as Infant Protectors in Hanuman Langurs (Presbytis entellus) Living in Multimale Groups - Defence Pattern, Paternity and Sexual Behaviour

Behavioral ecology and sociobiology, 1999-10, Vol.46 (5), p.350-356

1999

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Genetic predisposition to multiple sclerosis as revealed by immunoprinting

Annals of neurology, 1997-03, Vol.41 (3), p.341-352

1997

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Helicobacter pylori infection and polymorphisms in the tumor necrosis factor region

Electrophoresis, 1999-01, Vol.20 (8), p.1756-1761

1999

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Amplification of microsatellites adapted from human systems in faecal DNA of wild Hanuman langurs (Presbytis entellus)

Electrophoresis, 1998-06, Vol.19 (8-9), p.1356-1361

1998

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Analysis of an IFN-gamma gene (IFNG) polymorphism in multiple sclerosis in Europe: effect of population structure on association with disease

Journal of interferon & cytokine research, 1999-09, Vol.19 (9), p.1037-1046

1999

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On simple repetitive DNA sequences and complex diseases

Electrophoresis, 1997, Vol.18 (9), p.1577-1585

1997

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An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene

Diabetes (New York, N.Y.), 1998-05, Vol.47 (5), p.851-854

1998

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Coding versus intron variability : extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations

Human genetics, 1997-03, Vol.99 (3), p.399-406

1997

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On telomere shortening in soft-tissue tumors

Journal of cancer research and clinical oncology, 1998, Vol.124 (3-4), p.165-171

1998

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The paradox of MHC-DRB exon/intron evolution: alpha-helix and beta-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with beta-sheet codons

Journal of molecular evolution, 1993-09, Vol.37 (3), p.260-272

1993

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Expression of (cac)n/(gtg)n simple repetitive sequences in mRNA of human lymphocytes

Human genetics, 1994, Vol.93 (1), p.35-41

1994

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Multilocus fingerprinting and single locus analyses in the great tit for paternity determination

Electrophoresis, 1996, Vol.17 (10), p.1555-1558

1996

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Novel members and germline polymorphisms in the human T-cell receptor Vb6 family

Immunogenetics (New York), 1993, Vol.37 (4), p.257-265

1993

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Extensive gene flow in human populations as revealed by protein and microsatellite DNA markers

Human heredity, 1997-05, Vol.47 (3), p.165-172

1997

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Indirect gene diagnoses for complex (multifactorial) diseases-A review

Gene, 1995-06, Vol.159 (1), p.49-55

1995

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Indirect DNA/gene diagnoses via electrophoresis - an obsolete principle?

Electrophoresis, 1995, Vol.16 (1), p.683-690

1995

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Immunoprinting reveals different genetic bases for (auto)immune diseases

Electrophoresis, 1995, Vol.16 (1), p.1693-1697

1995

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Simple repetitive (GAA)n loci in the human genome

Electrophoresis, 1993, Vol.14 (1), p.973-977

1993

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Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25

Human genetics, 1993-12, Vol.92 (6), p.629-630

1993

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DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

Telomeric lengths and telomerase activity in liposarcomas

Friedreich's ataxia: Revision of the phenotype according to molecular genetics

Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14, and Y in various Eurasian populations

Males as Infant Protectors in Hanuman Langurs (Presbytis entellus) Living in Multimale Groups - Defence Pattern, Paternity and Sexual Behaviour

Genetic predisposition to multiple sclerosis as revealed by immunoprinting

Helicobacter pylori infection and polymorphisms in the tumor necrosis factor region

Amplification of microsatellites adapted from human systems in faecal DNA of wild Hanuman langurs (Presbytis entellus)

Analysis of an IFN-gamma gene (IFNG) polymorphism in multiple sclerosis in Europe: effect of population structure on association with disease

On simple repetitive DNA sequences and complex diseases

An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene

Coding versus intron variability : extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations

On telomere shortening in soft-tissue tumors

The paradox of MHC-DRB exon/intron evolution: alpha-helix and beta-sheet encoding regions diverge while hypervariable intronic simple repeats coevolve with beta-sheet codons

Expression of (cac)n/(gtg)n simple repetitive sequences in mRNA of human lymphocytes

Multilocus fingerprinting and single locus analyses in the great tit for paternity determination

Novel members and germline polymorphisms in the human T-cell receptor Vb6 family

Extensive gene flow in human populations as revealed by protein and microsatellite DNA markers

Indirect gene diagnoses for complex (multifactorial) diseases-A review

Indirect DNA/gene diagnoses via electrophoresis - an obsolete principle?

Immunoprinting reveals different genetic bases for (auto)immune diseases

Simple repetitive (GAA)n loci in the human genome

Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25

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