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Publications by Verena Steinke-Lange

Copy Number Variation Analysis and Targeted NGS in 77 Families With Suspected Lynch Syndrome Reveals Novel Potential Causative Genes

International Journal of Cancer

Cancer Research

English

BRAF Mutation Testing of MSI CRCs in Lynch Syndrome Diagnostics: Performance and Efficiency According to Patient`s Age

English

Related publications

Copy Number Variation Meta-Analysis Reveals a Novel Duplication at 9p24 Associated With Multiple Neurodevelopmental Disorders

Genome Medicine

Molecular Medicine

Molecular Biology

English

Targeted Deep Sequencing of Flowering Regulators in Brassica Napus Reveals Extensive Copy Number Variation

Scientific data

Information Sciences

Information Systems

Computer Science Applications

English

Rare Copy Number Variants Analysis Identifies Novel Candidate Genes in Heterotaxy Syndrome Patients With Congenital Heart Defects

Genome Medicine

Molecular Medicine

Molecular Biology

English

Germline Copy Number Variation Associated With Mendelian Inheritance of CLL in Two Families

Cancer Research

English

Copy Number Analysis Reveals a Novel Multiexon Deletion of theCOLQgene in Congenital Myasthenia

Neurology: Genetics

English

8p23.1 Duplication Syndrome Differentiated From Copy Number Variation of the Defensin Cluster at Prenatal Diagnosis in Four New Families

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

Clinical Characterization and Mutation Spectrum in Caribbean Hispanic Families With Lynch Syndrome

Familial Cancer

Cancer Research

English

Combined Mutation and Copy-Number Variation Detection by Targeted Next-Generation Sequencing in Uveal Melanoma

Modern Pathology

Forensic Medicine

English

Copy Number Variation in Patients With Cervical Artery Dissection

European Journal of Human Genetics

English