Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998

Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics.

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Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics.

Clinical epigenetics·2019

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.

Molecular psychiatry·2018

Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens.

Scientific reports·2017

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.

European journal of endocrinology·2015

Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome.

Clinical genetics·2015

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Cytogenetics and cell genetics·2012

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

Cytogenetics and cell genetics·2002

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

Cytogenetics and cell genetics·2002

The pattern of phylogenomic evolution of the Canidae.

Cytogenetics and cell genetics·2002

Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

Cytogenetics and cell genetics·2002

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Cytogenetics and cell genetics·2002

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Frontiers in endocrinology·2026

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Frontiers in psychiatry·2026

Compound Heterozygous PCDH15 Variants Associated With Cone-Rod Dystrophy in a Chinese Pedigree.

Molecular genetics & genomic medicine·2026

Genetically Predicted Muscle Mass and Function in Relation to Deep Vein Thrombosis: A Two-step Mendelian Randomization Study Highlighting the Mediating Role of BMI.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2026

Related Experiment Videos

Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998

Related Concept Videos

Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics.

Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics.

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.

Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens.

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.

Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome.

Gene mapping in marsupials and monotremes. II. Assignments to the X chromosome of dasyurid marsupials.

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.

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Analysis of chromosomal aberrations involving chromosome 1q31-->q53 in a DMBA-induced rat fibrosarcoma cell line: amplification and overexpression of Jak2.

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Compound Heterozygous PCDH15 Variants Associated With Cone-Rod Dystrophy in a Chinese Pedigree.

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Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998

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