Ascertainment of genetic disease in relatives of affected persons

The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century.

JAMA·2001

The sequence of the human genome.

Science (New York, N.Y.)·2001

Implications of the Human Genome Project for medical science.

JAMA·2001

Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis.

Clinical genetics·2000

Online Mendelian Inheritance in Man (OMIM).

Human mutation·1999

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.

Prenatal diagnosis·1999

Electroencephalography in the evaluation of headache patients: a review.

Israel journal of medical sciences·1998

Complementary medicine--a critical review.

Israel journal of medical sciences·1998

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Israel journal of medical sciences·1998

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

Israel journal of medical sciences·1998

A comparison between arterial- and venous-sampled activated clotting time measurements.

Israel journal of medical sciences·1998

Heart rate variability in patients with secondary amyloidosis.

Israel journal of medical sciences·1998

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

Ascertainment of genetic disease in relatives of affected persons

Related Concept Videos

The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century.

The sequence of the human genome.

Implications of the Human Genome Project for medical science.

Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis.

Online Mendelian Inheritance in Man (OMIM).

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.

Electroencephalography in the evaluation of headache patients: a review.

Complementary medicine--a critical review.

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

A comparison between arterial- and venous-sampled activated clotting time measurements.

Heart rate variability in patients with secondary amyloidosis.

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).

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

Related Experiment Videos

Ascertainment of genetic disease in relatives of affected persons

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