Mutation and linkage disequilibrium in human mtDNA

Estimation of relative fitnesses from relative risk data and the predicted future of haemoglobin alleles S and C.

Journal of evolutionary biology·2004

Evaluation of d2, a microsatellite measure of inbreeding and outbreeding, in wolves with a known pedigree.

Evolution; international journal of organic evolution·2001

Heterozygosity and fitness: no association in Scots pine.

Genetics·1995

Prognostic relevance of serum hyaluronan levels in patients with breast cancer.

International journal of cancer·1992

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

Genomics·1992

Acceptability trials with ready to eat foods in a rural area.

Indian pediatrics·1992

Unveiling ocular developmental disorders through short-read whole-genome sequencing.

European journal of human genetics : EJHG·2026

Family-oriented support in genetic counselling: a scoping review of clinical practice and psychotherapeutic interventions.

European journal of human genetics : EJHG·2026

Timothy syndrome and CACNA1C-Related Disorder: first international language and management guidelines consensus statement.

European journal of human genetics : EJHG·2026

Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

European journal of human genetics : EJHG·2026

Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost project.

European journal of human genetics : EJHG·2026

Whole-exome sequencing reveals novel and previously reported variants in genes linked to white matter pathology in neurodevelopmental disorders.

European journal of human genetics : EJHG·2026

A generalized test of genotype-phenotype causality in population-sampled nuclear families.

PLoS genetics·2026

Defining Haplosufficiency in Autosomal Recessive Limb-Girdle Muscular Dystrophy Using Molecular Markers in Disease Carriers.

Neurology. Genetics·2026

Low-Coverage Whole-Genome Sequencing Identifies Loci Associated with Birth Weight in East Friesian × Hu Crossbred Sheep.

Animals : an open access journal from MDPI·2026

Integrative MRI and Genomics Analyses Prioritize PACSIN1 as a Candidate Gene for Cerebellar Ataxia in Border Collies.

Animals : an open access journal from MDPI·2026

Bayesian Population-Based Prevalence Estimation of KCNV2-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.

International journal of molecular sciences·2026

Translatable electrophysiological and behavioral abnormalities in a humanized model of SYNGAP1-disorder.

Molecular psychiatry·2026

Related Experiment Videos

Mutation and linkage disequilibrium in human mtDNA

Related Concept Videos

Estimation of relative fitnesses from relative risk data and the predicted future of haemoglobin alleles S and C.

Evaluation of d2, a microsatellite measure of inbreeding and outbreeding, in wolves with a known pedigree.

Heterozygosity and fitness: no association in Scots pine.

Prognostic relevance of serum hyaluronan levels in patients with breast cancer.

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

Acceptability trials with ready to eat foods in a rural area.

Unveiling ocular developmental disorders through short-read whole-genome sequencing.

Family-oriented support in genetic counselling: a scoping review of clinical practice and psychotherapeutic interventions.

Timothy syndrome and CACNA1C-Related Disorder: first international language and management guidelines consensus statement.

Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost project.

Whole-exome sequencing reveals novel and previously reported variants in genes linked to white matter pathology in neurodevelopmental disorders.

A generalized test of genotype-phenotype causality in population-sampled nuclear families.

Defining Haplosufficiency in Autosomal Recessive Limb-Girdle Muscular Dystrophy Using Molecular Markers in Disease Carriers.

Low-Coverage Whole-Genome Sequencing Identifies Loci Associated with Birth Weight in East Friesian × Hu Crossbred Sheep.

Integrative MRI and Genomics Analyses Prioritize PACSIN1 as a Candidate Gene for Cerebellar Ataxia in Border Collies.

Bayesian Population-Based Prevalence Estimation of KCNV2-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.

Translatable electrophysiological and behavioral abnormalities in a humanized model of SYNGAP1-disorder.

Related Experiment Videos

Mutation and linkage disequilibrium in human mtDNA

Related Concept Videos

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