International System for Human Gene Nomenclature (1979) ISGN (1979)

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Genetic polymorphism of serum complement components in the chimpanzee.

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Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease.

Genes and immunity·2006

On the role of the starved codon and the takeoff site in ribosome bypassing in Escherichia coli.

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Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks.

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Limb anomalies from evolutionary, developmental, and genetic perspectives.

Birth defects original article series·1996

Multisite neural tube closure in humans.

Birth defects original article series·1996

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Bioinformation·2026

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Characteristics of a Cohort of Individuals With SCA27B Associated With Repeat Expansions in FGF14.

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Simultaneous quantitative detection of multiple low-frequency variants by high-dynamic-range capillary electrophoresis.

Molecular therapy. Nucleic acids·2026

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International System for Human Gene Nomenclature (1979) ISGN (1979)

Related Concept Videos

Drug and alcohol use, delinquency, and vandalism among upper middle class pre- and post-adolescents.

Genetic polymorphism of serum complement components in the chimpanzee.

Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease.

On the role of the starved codon and the takeoff site in ribosome bypassing in Escherichia coli.

HLA-Cw0409N is associated with HLA-A2301 and HLA-B*4403-carrying haplotypes.

Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks.

Limb anomalies from evolutionary, developmental, and genetic perspectives.

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Computational insights for target prioritization and pesticide effects on intrauterine growth restriction (IUGR).

Relationship between cardiac index and brain volume in the UK Biobank.

Characteristics of a Cohort of Individuals With SCA27B Associated With Repeat Expansions in FGF14.

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International System for Human Gene Nomenclature (1979) ISGN (1979)

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