[Chromosomal breakage in incontinentia pigmenti. Study of a family]

Dupilumab in Eosinophilic Gastrointestinal Disorders With Extraesophageal Involvement: A Pediatric Case Series and Systematic Review.

Journal of investigational allergology & clinical immunology·2025

Anaphylaxis to clindamycin following cutaneous exposure.

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology·2020

CSACI guidelines for the ethical, evidence-based and patient-oriented clinical practice of oral immunotherapy in IgE-mediated food allergy.

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology·2020

TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia.

Journal of clinical immunology·2019

Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.

Human genetics·2016

Consultation with registered dietitian to prevent accidental reactions to food: insight from an egg allergy influenza vaccination cohort.

European journal of clinical nutrition·2016

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

In mice, a population of male germ cells show characteristics of nonapoptotic cell death during G0 arrest.

Proceedings of the National Academy of Sciences of the United States of America·2026

Genome-wide mapping of Cas9-induced sister chromatid exchange across single and over 200 genomic sites in human cells.

eLife·2026

Wavelet-based whole genome doubling aware single-cell copy number calling.

Nucleic acids research·2026

Ki-67 regulates heterochromatin organization in neurons and forms condensates with heterochromatic components.

Nature communications·2026

Cell cycle-dependent chromatin motion: a role for DNA content doubling over cohesion.

Nucleic acids research·2026

Division Specific Biologically Effective Dose Predicts Gamma Knife Radiosurgery Outcomes in Multiple Sclerosis-Associated Trigeminal Neuralgia.

Neurosurgery practice·2026

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Dupilumab in Eosinophilic Gastrointestinal Disorders With Extraesophageal Involvement: A Pediatric Case Series and Systematic Review.

Anaphylaxis to clindamycin following cutaneous exposure.

CSACI guidelines for the ethical, evidence-based and patient-oriented clinical practice of oral immunotherapy in IgE-mediated food allergy.

TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia.

Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.

Consultation with registered dietitian to prevent accidental reactions to food: insight from an egg allergy influenza vaccination cohort.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

In mice, a population of male germ cells show characteristics of nonapoptotic cell death during G0 arrest.

Genome-wide mapping of Cas9-induced sister chromatid exchange across single and over 200 genomic sites in human cells.

Wavelet-based whole genome doubling aware single-cell copy number calling.

Ki-67 regulates heterochromatin organization in neurons and forms condensates with heterochromatic components.

Cell cycle-dependent chromatin motion: a role for DNA content doubling over cohesion.

Division Specific Biologically Effective Dose Predicts Gamma Knife Radiosurgery Outcomes in Multiple Sclerosis-Associated Trigeminal Neuralgia.

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