Advances in medical genetics: Huntington disease

Complex wavelet filter improves FLIM phasors for photon starved imaging experiments.

Biomedical optics express·2021

[Electrophoresis of rare earth elements on cellulose acetate].

Mikrochimica acta·2012

Familial cancer syndromes: catalog with comments.

Cytogenetic and genome research·2007

A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sample.

Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence·2002

Postexposure prophylaxis after nonoccupational HIV exposure: clinical, ethical, and policy considerations.

JAMA·1998

The journal "impact factor": a misnamed, misleading, misused measure.

Cancer genetics and cytogenetics·1998

Something Doesn't Look Right: Recognizing and Managing Limb-Length Discrepancy.

Pediatrics in review·2026

Hantavirus Infections in Children.

Pediatrics in review·2026

Childhood Attachment Patterns and Disorders.

Pediatrics in review·2026

Hemangiomas: Beyond the Skin.

Pediatrics in review·2026

Long-Term Complications of Sickle Cell Disease.

Pediatrics in review·2026

Posttraumatic Stress Disorder in Children and Adolescents.

Pediatrics in review·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

Advances in medical genetics: Huntington disease

Related Concept Videos

Complex wavelet filter improves FLIM phasors for photon starved imaging experiments.

[Electrophoresis of rare earth elements on cellulose acetate].

Familial cancer syndromes: catalog with comments.

A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sample.

Postexposure prophylaxis after nonoccupational HIV exposure: clinical, ethical, and policy considerations.

The journal "impact factor": a misnamed, misleading, misused measure.

Something Doesn't Look Right: Recognizing and Managing Limb-Length Discrepancy.

Hantavirus Infections in Children.

Childhood Attachment Patterns and Disorders.

Hemangiomas: Beyond the Skin.

Long-Term Complications of Sickle Cell Disease.

Posttraumatic Stress Disorder in Children and Adolescents.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

Advances in medical genetics: Huntington disease

Related Concept Videos

Related Articles