Single copy probe CRI-L114 (D4S110) maps to 4p16.1

Clinical characteristics of women with HIV in the RESPOND cohort: A descriptive analysis and comparison to men.

HIV medicine·2024

Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation.

Muscle & nerve. Supplement·2013

Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindreds.

Journal of lipid research·2000

Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorder.

The American journal of psychiatry·1999

Genetic polymorphism of CYP2D6 and lung cancer risk.

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology·1998

Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium.

Annals of neurology·1998

Comprehensive post-transcriptional modification profiles in individual Staphylococcus aureus tRNA species.

Nucleic acids research·2026

Functional analysis of natural variation in the RNA-binding protein CsrA across the bacterial domain predicts regulatory activity.

Nucleic acids research·2026

miRNA-mediated cell-to-cell communications boost DNA repair during the radioadaptive response.

Nucleic acids research·2026

Synonymous mutations in essential genes infrequently produce fitness effects in human cell lines.

Nucleic acids research·2026

Classification of Sir2-HerA systems reveals a multilayered regulatory cascade gating the type III antiphage activity.

Nucleic acids research·2026

BASELINE: a CRISPR base editing platform for mammalian-scale single-cell lineage tracing.

Nucleic acids research·2026

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

Cureus·2026

The utilization of multiplex PCR with fragment analysis for carrier screening of spinal muscular atrophy.

Clinica chimica acta; international journal of clinical chemistry·2026

The Clinical Phenotype and Genetic Analysis of Monogenic Non Syndromic Obesity Caused by MC4R Gene Variation.

Molecular genetics & genomic medicine·2026

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Single copy probe CRI-L114 (D4S110) maps to 4p16.1

Related Concept Videos

Clinical characteristics of women with HIV in the RESPOND cohort: A descriptive analysis and comparison to men.

Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation.

Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindreds.

Dopamine D4 gene 7-repeat allele and attention deficit hyperactivity disorder.

Genetic polymorphism of CYP2D6 and lung cancer risk.

Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium.

Comprehensive post-transcriptional modification profiles in individual Staphylococcus aureus tRNA species.

Functional analysis of natural variation in the RNA-binding protein CsrA across the bacterial domain predicts regulatory activity.

miRNA-mediated cell-to-cell communications boost DNA repair during the radioadaptive response.

Synonymous mutations in essential genes infrequently produce fitness effects in human cell lines.

Classification of Sir2-HerA systems reveals a multilayered regulatory cascade gating the type III antiphage activity.

BASELINE: a CRISPR base editing platform for mammalian-scale single-cell lineage tracing.

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

The utilization of multiplex PCR with fragment analysis for carrier screening of spinal muscular atrophy.

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Single copy probe CRI-L114 (D4S110) maps to 4p16.1

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