[Major genes, modifying genes, and environmental effect of Duchenne de Boulogne myopathy]

Rectal swab testing before prostate biopsy: experience in a VA Medical Center urology practice.

Prostate cancer and prostatic diseases·2015

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

Revue neurologique·2015

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

Placenta·2014

The presymptomatic phase of Huntington disease.

Revue neurologique·2012

[Critical approach to clinical trials: difficulties of such research in Lebanon].

Revue neurologique·2012

A one year prevalence study of schizophrenia on Reunion Island.

European psychiatry : the journal of the Association of European Psychiatrists·2009

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

Gene-Corrected Human iPSC-Derived Cardiomyocytes and Skeletal Muscles Reveal Partial Dystrophin Dp427 Preservation and Cardiac Dp116 Expression in Duchenne Muscular Dystrophy Patient With a Splice-Site Mutation in Intron 68 (c.9975-1G>T).

Circulation. Genomic and precision medicine·2026

From free text to structured genomics: future-proofing cancer registries for precision oncology.

ESMO real world data and digital oncology·2026

Investigation of allele-specific expression in citrus hybrids reveals the association between siRNA-mediated de novo methylation and high expression in citrus genomes.

Horticulture research·2026

Protective IFIH1 variant reduces islet stress and dysfunction in a type 1 diabetes genetic background.

iScience·2026

A lipid metabolism-based gene signature defines diagnosis and molecular heterogeneity in diabetic nephropathy.

Iranian journal of basic medical sciences·2026

Whole Genome Sequencing of Discordant Monozygotic Twins Reveals Regulatory Variants Associated With Nonsyndromic Orofacial Clefts.

Human mutation·2026

Related Experiment Videos

[Major genes, modifying genes, and environmental effect of Duchenne de Boulogne myopathy]

Related Concept Videos

Rectal swab testing before prostate biopsy: experience in a VA Medical Center urology practice.

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

The presymptomatic phase of Huntington disease.

[Critical approach to clinical trials: difficulties of such research in Lebanon].

A one year prevalence study of schizophrenia on Reunion Island.

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.

Gene-Corrected Human iPSC-Derived Cardiomyocytes and Skeletal Muscles Reveal Partial Dystrophin Dp427 Preservation and Cardiac Dp116 Expression in Duchenne Muscular Dystrophy Patient With a Splice-Site Mutation in Intron 68 (c.9975-1G>T).

From free text to structured genomics: future-proofing cancer registries for precision oncology.

Investigation of allele-specific expression in citrus hybrids reveals the association between siRNA-mediated de novo methylation and high expression in citrus genomes.

Protective IFIH1 variant reduces islet stress and dysfunction in a type 1 diabetes genetic background.

A lipid metabolism-based gene signature defines diagnosis and molecular heterogeneity in diabetic nephropathy.

Whole Genome Sequencing of Discordant Monozygotic Twins Reveals Regulatory Variants Associated With Nonsyndromic Orofacial Clefts.

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[Major genes, modifying genes, and environmental effect of Duchenne de Boulogne myopathy]

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