Interstitial telomere DNA sequences are not detectable at breaking sites of classical heritable fragile sites

French multicentre prospective evaluation of radiofrequency ablation in the management of haemorrhoidal disease.

Techniques in coloproctology·2023

[Uterine rupture in a patient with a cesarean scar pregnancy].

Revue medicale de Liege·2022

[Alcohol, pregnancy and breast-feeding].

Revue medicale de Liege·2019

Online training on how to diagnose anoperineal lesions of Crohn's disease: Do pictures matter? A nationwide randomized study.

Clinics and research in hepatology and gastroenterology·2019

Doppler ultrasound in the diagnosis of Budd-Chiari syndrome in children after split liver transplantation.

Diagnostic and interventional imaging·2018

The first joint ESGAR/ ESPR consensus statement on the technical performance of cross-sectional small bowel and colonic imaging.

European radiology·2016

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Human genetics·2026

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

Identification of the HLA-DQB1*03:626 Allele in Two Individuals in a Western Indian Family.

HLA·2026

Sporadic Retinal Astrocytic Hamartoma Mimicking Retinoblastoma in a Child: A Case Report and Literature Review.

Clinical case reports·2026

Primary Care Recognition of Rabson-Mendenhall Syndrome Despite Absence of Classical Diabetic Symptoms.

The American journal of case reports·2026

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

HLA·2026

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

HLA·2026

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

HLA·2026

Related Experiment Videos

Interstitial telomere DNA sequences are not detectable at breaking sites of classical heritable fragile sites

Related Concept Videos

French multicentre prospective evaluation of radiofrequency ablation in the management of haemorrhoidal disease.

[Uterine rupture in a patient with a cesarean scar pregnancy].

[Alcohol, pregnancy and breast-feeding].

Online training on how to diagnose anoperineal lesions of Crohn's disease: Do pictures matter? A nationwide randomized study.

Doppler ultrasound in the diagnosis of Budd-Chiari syndrome in children after split liver transplantation.

The first joint ESGAR/ ESPR consensus statement on the technical performance of cross-sectional small bowel and colonic imaging.

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

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Identification of the HLA-DQB1*03:626 Allele in Two Individuals in a Western Indian Family.

Sporadic Retinal Astrocytic Hamartoma Mimicking Retinoblastoma in a Child: A Case Report and Literature Review.

Primary Care Recognition of Rabson-Mendenhall Syndrome Despite Absence of Classical Diabetic Symptoms.

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

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Related Experiment Videos

Interstitial telomere DNA sequences are not detectable at breaking sites of classical heritable fragile sites

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