TIGR/MYOC proximal promoter GT-repeat polymorphism is not associated with myopia

[Echocardiographic characteristics and prognostic evaluation of Ebstein anomaly in fetuses].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2025

[Follow-up study of fetal cardiac birth defects after prenatal diagnosis and graded counseling].

Zhonghua fu chan ke za zhi·2022

[Prenatal interventional therapy in two cases with critical pulmonary stenosis or pulmonary atresia with intact ventricular septum].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2018

SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.

The pharmacogenomics journal·2017

Micromechanical Origin of Particle Size Segregation.

Physical review letters·2017

Characterization of base roughness for granular chute flows.

Physical review. E·2016

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Human mutation·2026

Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

Human mutation·2026

Mutation Severity of FBXO43 Determines Spermatogenic Outcome and Informs Precision ART Strategies.

Human mutation·2026

Mitochondrial tRNASer(AGY) 12234A > G Mutation May Contribute to the Clinical Expression of Hypertrophic Cardiomyopathy-Associated tRNAIle 4263A > G Mutation.

Human mutation·2026

Splice effect of a synonymous variant in AP4B1: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia.

Human mutation·2026

Integrated Mutation Profiling and Prognostic Genomic Signature in Pediatric Testicular and Ovarian Germ Cell Tumors.

Human mutation·2026

Characterisation of the Novel HLA-C*08:334 Allele in a Brazilian Volunteer Donor.

HLA·2026

Identification of the Novel HLA-DQB1*05:385 Allele Through Next-Generation Sequencing.

HLA·2026

Uncommon Concurrent Retinal and Cerebral Metastasis in High-risk Neuroblastoma: Diagnostic Utility of 68Ga-DOTATATE PET/CT Despite Negative 18F-FDG PET/CT.

Clinical nuclear medicine·2026

Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

HLA·2026

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

International journal of molecular sciences·2026

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

HLA·2026

Related Experiment Videos

TIGR/MYOC proximal promoter GT-repeat polymorphism is not associated with myopia

Related Concept Videos

[Echocardiographic characteristics and prognostic evaluation of Ebstein anomaly in fetuses].

[Follow-up study of fetal cardiac birth defects after prenatal diagnosis and graded counseling].

[Prenatal interventional therapy in two cases with critical pulmonary stenosis or pulmonary atresia with intact ventricular septum].

SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.

Micromechanical Origin of Particle Size Segregation.

Characterization of base roughness for granular chute flows.

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

Mutation Severity of FBXO43 Determines Spermatogenic Outcome and Informs Precision ART Strategies.

Mitochondrial tRNASer(AGY) 12234A > G Mutation May Contribute to the Clinical Expression of Hypertrophic Cardiomyopathy-Associated tRNAIle 4263A > G Mutation.

Splice effect of a synonymous variant in AP4B1: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia.

Integrated Mutation Profiling and Prognostic Genomic Signature in Pediatric Testicular and Ovarian Germ Cell Tumors.

Characterisation of the Novel HLA-C*08:334 Allele in a Brazilian Volunteer Donor.

Identification of the Novel HLA-DQB1*05:385 Allele Through Next-Generation Sequencing.

Uncommon Concurrent Retinal and Cerebral Metastasis in High-risk Neuroblastoma: Diagnostic Utility of 68Ga-DOTATATE PET/CT Despite Negative 18F-FDG PET/CT.

Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

Related Experiment Videos

TIGR/MYOC proximal promoter GT-repeat polymorphism is not associated with myopia

Related Concept Videos

Related Articles