An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.

Nature communications·2019

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

Molecular psychiatry·2012

Towards an evidence-based process for the clinical interpretation of copy number variation.

Clinical genetics·2011

Molecular cytogenetic analysis of telomere rearrangements.

Current protocols in human genetics·2008

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Journal of medical genetics·2005

Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.

American journal of medical genetics. Part A·2005

The MODNAP benchmark set for modeling ribose-based modified nucleic acid and nucleic acid-protein complexes: a case study with AlphaFold 3.

Nucleic acids research·2026

Chemically stabilized long antisense oligonucleotides perturb RNA exosome function.

Nucleic acids research·2026

CLEAN Database: providing enzyme function coverage for over 55 million sequences.

Nucleic acids research·2026

DRAMP 5.0: an update integrating sequence and structure in a novel FASTS format for AI-driven design of antimicrobial peptides.

Nucleic acids research·2026

OAS-nano: the Observed VHH Space Database.

Nucleic acids research·2026

Structural basis of assembly-dependent activation of the MAD3-MAD4 nuclease in the Pseudomonas aeruginosa MADS defense system.

Nucleic acids research·2026

Genome-Wide Identification of the BhKCS Gene Family in Wax Gourd (Benincasa hispida) and Stress-Responsive Expression of BhKCS8/9/14/15.

Plants (Basel, Switzerland)·2026

Selection and Validation of Reference Genes for RT-qPCR Across Different Organs, Flower Bud Developmental Stages, and Hormone Treatments in Ilex verticillata.

Plants (Basel, Switzerland)·2026

Phenotypic Complexity and Diagnostic Utility of Exome Sequencing in ASD: Real-World Insights from Colombia.

International journal of molecular sciences·2026

Unveiling Glial Heterogeneity in the Inner Retina: Non-Visual Photic Spectrum Responses and Calcium Dynamics in Müller Glial Cells vs. Neurons.

International journal of molecular sciences·2026

Pathway-Level Synthesis Reveals Contrast-Dependent Rat Brain Transcriptomic Responses to Alcohol.

International journal of molecular sciences·2026

Population Frequencies of VWD-Associated Genotypes: Cross-Resource Evidence from RGC-ME and gnomAD.

International journal of molecular sciences·2026

Related Experiment Videos

An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]

Related Concept Videos

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

Towards an evidence-based process for the clinical interpretation of copy number variation.

Molecular cytogenetic analysis of telomere rearrangements.

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.

The MODNAP benchmark set for modeling ribose-based modified nucleic acid and nucleic acid-protein complexes: a case study with AlphaFold 3.

Chemically stabilized long antisense oligonucleotides perturb RNA exosome function.

CLEAN Database: providing enzyme function coverage for over 55 million sequences.

DRAMP 5.0: an update integrating sequence and structure in a novel FASTS format for AI-driven design of antimicrobial peptides.

OAS-nano: the Observed VHH Space Database.

Structural basis of assembly-dependent activation of the MAD3-MAD4 nuclease in the Pseudomonas aeruginosa MADS defense system.

Genome-Wide Identification of the BhKCS Gene Family in Wax Gourd (Benincasa hispida) and Stress-Responsive Expression of BhKCS8/9/14/15.

Selection and Validation of Reference Genes for RT-qPCR Across Different Organs, Flower Bud Developmental Stages, and Hormone Treatments in Ilex verticillata.

Phenotypic Complexity and Diagnostic Utility of Exome Sequencing in ASD: Real-World Insights from Colombia.

Unveiling Glial Heterogeneity in the Inner Retina: Non-Visual Photic Spectrum Responses and Calcium Dynamics in Müller Glial Cells vs. Neurons.

Pathway-Level Synthesis Reveals Contrast-Dependent Rat Brain Transcriptomic Responses to Alcohol.

Population Frequencies of VWD-Associated Genotypes: Cross-Resource Evidence from RGC-ME and gnomAD.

Related Experiment Videos

An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]

Related Concept Videos

Related Articles