Fragile sites and chromosome breakpoints in constitutional rearrangements

The MLL recombinome of acute leukemias in 2017.

Leukemia·2017

Sperm RNA preparation for transcriptomic analysis: Review of the techniques and personal experience.

Andrologia·2017

[Congenital bilateral absence of vas deferens: From diagnosis to assisted reproductive techniques - the experience of three centers].

Gynecologie, obstetrique & fertilite·2015

Balanced complex chromosome rearrangement in male infertility: case report and literature review.

Andrologia·2014

DNA fragmentation is higher in spermatozoa with chromosomally unbalanced content in men with a structural chromosomal rearrangement.

Andrology·2013

The MLL recombinome of acute leukemias in 2013.

Leukemia·2013

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Clinical genetics·2026

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Clinical genetics·2026

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Clinical genetics·2026

Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Clinical genetics·2026

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Molecular biology of the cell·2026

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Methods in molecular biology (Clifton, N.J.)·2026

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

Nature structural & molecular biology·2026

Resolving missing human polymorphic inversions and other complex variants from ultra-long read data.

Genome research·2026

Mitochondrial Complex I at the Crossroads of NK cell Dysfunction in Glioblastoma.

Cancer discovery·2026

A Novel Sparse Cellular Labeling System with Tunable Gradients and Long-Term Stability.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

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Fragile sites and chromosome breakpoints in constitutional rearrangements

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The MLL recombinome of acute leukemias in 2017.

Sperm RNA preparation for transcriptomic analysis: Review of the techniques and personal experience.

[Congenital bilateral absence of vas deferens: From diagnosis to assisted reproductive techniques - the experience of three centers].

Balanced complex chromosome rearrangement in male infertility: case report and literature review.

DNA fragmentation is higher in spermatozoa with chromosomally unbalanced content in men with a structural chromosomal rearrangement.

The MLL recombinome of acute leukemias in 2013.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

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Enhancing Diagnostic Precision in Non-Immune Hydrops Fetalis: The Incremental Value of Whole Exome Sequencing-A Prospective Cohort Study.

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

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