Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction

Congenital heart defects in the recurrent 2q13 deletion syndrome.

European journal of medical genetics·2021

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Clinical genetics·2018

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Clinical genetics·2018

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Clinical genetics·2017

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Clinical genetics·2017

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

Molecular syndromology·2013

Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island.

Human genetics·2026

Clinical and molecular spectrum of congenital disorders of glycosylation in 80 Egyptian patients.

Human genetics·2026

Annual average exposure to ambient air pollution, polygenic risk, and incidence of major chronic diseases: a large-scale prospective cohort study.

Human genetics·2026

Association of apolipoprotein E gene with risk, cognition, and prognosis of epilepsy.

Human genetics·2026

A case-control study on IL-8 gene polymorphisms and serum IL-8 levels in patients with age-related macular degeneration in India.

Human genetics·2026

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Human genetics·2026

Genomic models for accurate estimation of breeding values in Sitka spruce (Picea sitchensis Bong. Carr).

Heredity·2026

Implementing genetics-based cascade testing for familial hypercholesterolemia in Colombia: Results from a pilot study and implications for national screening strategies.

Journal of clinical lipidology·2026

Combined linkage mapping and association analysis reveal the genetic control of starch content in maize kernel.

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

Expanding Clinical and Variant Spectrum of CBX1-Related Syndrome: Report of Three Novel Cases.

Clinical genetics·2026

The complete mitochondrial genome of Neomyia gavisa (Walker, 1859) (Diptera: Muscidae).

Mitochondrial DNA. Part B, Resources·2026

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Related Experiment Videos

Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction

Related Concept Videos

Congenital heart defects in the recurrent 2q13 deletion syndrome.

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island.

Clinical and molecular spectrum of congenital disorders of glycosylation in 80 Egyptian patients.

Annual average exposure to ambient air pollution, polygenic risk, and incidence of major chronic diseases: a large-scale prospective cohort study.

Association of apolipoprotein E gene with risk, cognition, and prognosis of epilepsy.

A case-control study on IL-8 gene polymorphisms and serum IL-8 levels in patients with age-related macular degeneration in India.

Clinical, immunological, and molecular characteristics of severe combined immune deficiency in China.

Genomic models for accurate estimation of breeding values in Sitka spruce (Picea sitchensis Bong. Carr).

Implementing genetics-based cascade testing for familial hypercholesterolemia in Colombia: Results from a pilot study and implications for national screening strategies.

Combined linkage mapping and association analysis reveal the genetic control of starch content in maize kernel.

Expanding Clinical and Variant Spectrum of CBX1-Related Syndrome: Report of Three Novel Cases.

The complete mitochondrial genome of Neomyia gavisa (Walker, 1859) (Diptera: Muscidae).

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Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction

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