Distribution of CAG repeats in normal and Huntington's disease patients in Israel

Plasticity of Dental Cell Types in Development, Regeneration, and Evolution.

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Schweizer Archiv fur Tierheilkunde·2022

Deterioration of specific aspects of gait during the instrumented 6-min walk test among people with multiple sclerosis.

Journal of neurology·2019

A new approach to quantifying the EEG during walking: Initial evidence of gait related potentials and their changes with aging and dual tasking.

Experimental gerontology·2019

Age-associated changes in obstacle negotiation strategies: Does size and timing matter?

Gait & posture·2017

Triple paternal contribution to a normal/complete molar chimeric singleton placenta.

Human reproduction (Oxford, England)·2017

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

Clinical genetics·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

Clinical genetics·2026

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Clinical genetics·2026

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

Clinical genetics·2026

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Clinical genetics·2026

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Human genetics·2026

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Diagnostics (Basel, Switzerland)·2026

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Drug delivery·2026

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Frontiers in plant science·2026

Rapid and Sensitive Detection of USP26 Cluster Variants Based on CRISPR/Cas12a.

Human mutation·2026

Integrative long-read sequencing, RNA-seq and machine learning framework characterizes and predicts autosomal silencing in unbalanced X-autosome translocations.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Related Experiment Videos

Distribution of CAG repeats in normal and Huntington's disease patients in Israel

Related Concept Videos

Plasticity of Dental Cell Types in Development, Regeneration, and Evolution.

[Is alfalfa hay an alternative to meadow hay in equine nutrition?]

Deterioration of specific aspects of gait during the instrumented 6-min walk test among people with multiple sclerosis.

A new approach to quantifying the EEG during walking: Initial evidence of gait related potentials and their changes with aging and dual tasking.

Age-associated changes in obstacle negotiation strategies: Does size and timing matter?

Triple paternal contribution to a normal/complete molar chimeric singleton placenta.

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

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

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Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

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Related Experiment Videos

Distribution of CAG repeats in normal and Huntington's disease patients in Israel

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