Gene mapping and chromosome 21: history and methodology

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

Annals of human genetics·1994

The CEPH consortium linkage map of human chromosome 2.

Genomics·1992

The CEPH consortium primary linkage map of human chromosome 10.

Genomics·1990

The human gene map.

Philosophical transactions of the Royal Society of London. Series B, Biological sciences·1988

Platelet-collagen interaction: inhibition by ristocetin and enhancement by von Willebrand factor-platelet binding.

Blood·1986

A genetic map of chromosome 19 based on family linkage data.

Annals of human genetics·1985

20 years later.

Human genetics. Supplement·1981

Asking for a prenatal diagnosis after the birth of a child with Down's syndrome.

Human genetics. Supplement·1981

Pathology of trisomy 21--with particular reference to persistent common atrioventricular canal of the heart.

Human genetics. Supplement·1981

Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.

Human genetics. Supplement·1981

Down's syndrome: problems of immunodeficiency.

Human genetics. Supplement·1981

Clinical aspects of Down's syndrome from infancy to adult life.

Human genetics. Supplement·1981

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

bioRxiv : the preprint server for biology·2026

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

bioRxiv : the preprint server for biology·2026

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genomics, proteomics & bioinformatics·2026

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Nature communications·2026

Related Experiment Videos

Gene mapping and chromosome 21: history and methodology

Related Concept Videos

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

The CEPH consortium linkage map of human chromosome 2.

The CEPH consortium primary linkage map of human chromosome 10.

The human gene map.

Platelet-collagen interaction: inhibition by ristocetin and enhancement by von Willebrand factor-platelet binding.

A genetic map of chromosome 19 based on family linkage data.

20 years later.

Asking for a prenatal diagnosis after the birth of a child with Down's syndrome.

Pathology of trisomy 21--with particular reference to persistent common atrioventricular canal of the heart.

Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.

Down's syndrome: problems of immunodeficiency.

Clinical aspects of Down's syndrome from infancy to adult life.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Proteome-wide QTL mapping enables gene-protein-phenotype metabolic network construction in a genetically diverse MASLD mouse model.

Sequence determinants of pathogenicity in glucose-6-phosphatase linked to glycogen storage disease type 1a.

Estimating the Penetrance of PRNP Mutations in Chinese Prion Disease Patients based on the Genome Databases.

Genome-wide linkage and association mapping identified a novel candidate gene, TaGLK-A1, underlying fructan content in wheat grain.

Deletion of ARPKD-associated Pkhd1 gene in mice results in decreased Tfap2b expression and eye abnormalities.

Related Experiment Videos

Gene mapping and chromosome 21: history and methodology

Related Concept Videos

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