[Advances in genetics of retinoblastoma]

Prestin autoantibodies screening in idiopathic sudden sensorineural hearing loss.

European annals of otorhinolaryngology, head and neck diseases·2019

Association of dental and maxillary sinus pathologies with ear, nose, and throat symptoms.

Oral diseases·2017

Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.

Clinical genetics·2017

Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2017

Stable knockdown of CREB, HIF-1 and HIF-2 by replication-competent retroviruses abrogates the responses to hypoxia in hepatocellular carcinoma.

Cancer gene therapy·2016

CD48 on blood leukocytes and in serum of asthma patients varies with severity.

Allergy·2016

[Oculoplastics and Orbital Surgery Section: Orbital Fractures].

Harefuah·2026

[Atypical Presentation of Extensive Aortic Dissection: Lessons from a Silent Killer].

Harefuah·2026

[Eyeball or Eye Wheel?]

Harefuah·2026

[Emerging Trends in Pediatric rheumatology: Key Insights from the PReS 2025 European Congress - Helsinki, Finland, September 2025].

Harefuah·2026

[The Laterality of Endometriosis].

Harefuah·2026

[OASIS: Long-Term Implications on Women's Quality of Life].

Harefuah·2026

Genetic determinants that permit growth without the core septin Cdc12 in Cryptococcus neoformans.

G3 (Bethesda, Md.)·2026

Genome-wide identification of GhAOX gene family and its expression and regulation in cotton CMS line Jin A.

Frontiers in plant science·2026

Evaluating high-fidelity CRISPR-Cas nucleases in nucleosomal contexts using a quantitative framework.

Frontiers in genome editing·2026

Protein-protein interaction network architecture of human polygenic traits reveals domain-spanning connectivity and evolutionary pressures.

Genome biology·2026

Robust annotation and discovery of novel cell types in single-cell ATAC-seq data through cross-modal reference alignment.

Genome research·2026

Constitutional Ring Chromosomes in Greek Pediatric Patients: A 50-year Single-center Cytogenetic Study.

In vivo (Athens, Greece)·2026

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[Advances in genetics of retinoblastoma]

Related Concept Videos

Prestin autoantibodies screening in idiopathic sudden sensorineural hearing loss.

Association of dental and maxillary sinus pathologies with ear, nose, and throat symptoms.

Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.

Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.

Stable knockdown of CREB, HIF-1 and HIF-2 by replication-competent retroviruses abrogates the responses to hypoxia in hepatocellular carcinoma.

CD48 on blood leukocytes and in serum of asthma patients varies with severity.

[Oculoplastics and Orbital Surgery Section: Orbital Fractures].

[Atypical Presentation of Extensive Aortic Dissection: Lessons from a Silent Killer].

[Eyeball or Eye Wheel?]

[Emerging Trends in Pediatric rheumatology: Key Insights from the PReS 2025 European Congress - Helsinki, Finland, September 2025].

[The Laterality of Endometriosis].

[OASIS: Long-Term Implications on Women's Quality of Life].

Genetic determinants that permit growth without the core septin Cdc12 in Cryptococcus neoformans.

Genome-wide identification of GhAOX gene family and its expression and regulation in cotton CMS line Jin A.

Evaluating high-fidelity CRISPR-Cas nucleases in nucleosomal contexts using a quantitative framework.

Protein-protein interaction network architecture of human polygenic traits reveals domain-spanning connectivity and evolutionary pressures.

Robust annotation and discovery of novel cell types in single-cell ATAC-seq data through cross-modal reference alignment.

Constitutional Ring Chromosomes in Greek Pediatric Patients: A 50-year Single-center Cytogenetic Study.

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