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

Cerebral Ventriculomegaly With Abnormality of the Aqueduct of Sylvius: A Case Series.

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A Familial Case of Thauvin-Robinet-Faivre Syndrome (TROFAS), Presenting With Postaxial Polydactyly and Upper Lip Vascular Malformation.

Clinical genetics·2026

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

Loss-of-function variants in CFAP57, SEPTIN4, SPEM2, and CFAP46 cause asthenoteratozoospermia.

Human reproduction (Oxford, England)·2026

Chromosome-Scale Assembly of Novel Caenorhabditis sp. 65 (strain JU4118).

microPublication biology·2026

Comparative analysis of chromosome interaction networks in 12 human cell types using Hi-C.

Yi chuan = Hereditas·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

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

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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.

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

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Chromosome-Scale Assembly of Novel Caenorhabditis sp. 65 (strain JU4118).

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

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