A new pedigree with recessive mapping to CHED2 locus on 20p13

Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes.

Journal of dental research·2023

Associations with baseline visual acuity in 12,414 eyes starting treatment for neovascular AMD.

Eye (London, England)·2022

Thymus vulgaris essential oil and thymol inhibit biofilms and interact synergistically with antifungal drugs against drug resistant strains of Candida albicans and Candida tropicalis.

Journal de mycologie medicale·2020

Age, body weight and ovarian function affect oocyte size and morphology in non-PCOS patients undergoing intracytoplasmic sperm injection (ICSI).

PloS one·2019

Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta.

Journal of dental research·2019

Hemodynamic Impairment Measured by Positron-Emission Tomography Is Regionally Associated with Decreased Cortical Thickness in Moyamoya Phenomenon.

AJNR. American journal of neuroradiology·2018

Automated AI quantification of retinal parameters associated with axial length progression in children: a cohort study.

The British journal of ophthalmology·2026

Interaction of genetic susceptibility and sunlight exposure on primary open-angle glaucoma risk and progression.

The British journal of ophthalmology·2026

Posterior capsular rupture and phacoemulsification device.

The British journal of ophthalmology·2026

Association between retinal/choroidal vascularity and macular sensitivity in myopic macular degeneration: Aier-SERI high myopia adult cohort study.

The British journal of ophthalmology·2026

Pythium keratitis: experience from Thailand.

The British journal of ophthalmology·2026

Association of fenofibrate use with progression of ocular disease in individuals with diabetes.

The British journal of ophthalmology·2026

Integrative Principal Component-QTL Mapping Identifies Genetic Modifiers of Tumor and Metabolic Traits in Smad4-Deficient Collaborative Cross Mice.

International journal of molecular sciences·2026

Molecular Genetic Diagnosis of Spinal Muscular Atrophy: Clinical Utility, Challenges, and Lessons Learned from Illustrative Cases in a Single Center.

Genes·2026

Strictosidine Synthase-like Gene NMS1 Is Required for Male Fertility in Rice by Regulating Tapetal Degradation.

Genes·2026

Population-Specific Genetic Markers of Prostate Cancer Risk in Kazakh Men: Association Analysis of 102 SNPs and Risk Prediction Modeling.

Genes·2026

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

American journal of medical genetics. Part A·2026

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·2026

Related Experiment Videos

A new pedigree with recessive mapping to CHED2 locus on 20p13

Related Concept Videos

Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes.

Associations with baseline visual acuity in 12,414 eyes starting treatment for neovascular AMD.

Thymus vulgaris essential oil and thymol inhibit biofilms and interact synergistically with antifungal drugs against drug resistant strains of Candida albicans and Candida tropicalis.

Age, body weight and ovarian function affect oocyte size and morphology in non-PCOS patients undergoing intracytoplasmic sperm injection (ICSI).

Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta.

Hemodynamic Impairment Measured by Positron-Emission Tomography Is Regionally Associated with Decreased Cortical Thickness in Moyamoya Phenomenon.

Automated AI quantification of retinal parameters associated with axial length progression in children: a cohort study.

Interaction of genetic susceptibility and sunlight exposure on primary open-angle glaucoma risk and progression.

Posterior capsular rupture and phacoemulsification device.

Association between retinal/choroidal vascularity and macular sensitivity in myopic macular degeneration: Aier-SERI high myopia adult cohort study.

Pythium keratitis: experience from Thailand.

Association of fenofibrate use with progression of ocular disease in individuals with diabetes.

Integrative Principal Component-QTL Mapping Identifies Genetic Modifiers of Tumor and Metabolic Traits in Smad4-Deficient Collaborative Cross Mice.

Molecular Genetic Diagnosis of Spinal Muscular Atrophy: Clinical Utility, Challenges, and Lessons Learned from Illustrative Cases in a Single Center.

Strictosidine Synthase-like Gene NMS1 Is Required for Male Fertility in Rice by Regulating Tapetal Degradation.

Population-Specific Genetic Markers of Prostate Cancer Risk in Kazakh Men: Association Analysis of 102 SNPs and Risk Prediction Modeling.

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

Wilson disease associated with a novel variant in the ATP7B gene.

Related Experiment Videos

A new pedigree with recessive mapping to CHED2 locus on 20p13

Related Concept Videos

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