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Publications by Oliver Bartsch

Targeted Next-Generation Sequencing Analysis in Couples at Increased Risk for Autosomal Recessive Disorders

Orphanet Journal of Rare Diseases

English

Confirmation of EP300 Gene Mutations as a Rare Cause of Rubinstein–Taybi Syndrome

European Journal of Human Genetics

Genetics

2007

English

Related publications

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

Molecular Medicine Reports

English

Autosomal Recessive Congenital Ichthyosis: CERS3 Mutations Identified by a Next Generation Sequencing Panel Targeting Ichthyosis Genes

European Journal of Human Genetics

Genetics

2017

English

Targeted Therapy According to Next Generation Sequencing-Based Panel Sequencing

Fukushima Journal of Medical Sciences

Medicine

2018

English

Lessons From Next-Generation Sequencing in Genetic Skeletal Disorders

BoneKEy Reports

2014

English

Targeted Sequencing of Cancer-Associated Genes in Hepatocellular Carcinoma Using Next Generation Sequencing

Molecular Medicine Reports

English

Mutation Analysis of Nine Chordoma Specimens by Targeted Next-Generation Cancer Panel Sequencing

Journal of Cancer

Oncology

2015

English

Incidental Diagnosis of a Parental Balanced Reciprocal Rearrangement in Couples Undergoing Routine Aneuploidy Screening by Targeted Next Generation Sequencing (TNGS)

Fertility and Sterility

Gynecology

Reproductive Medicine

Obstetrics

2017

English

Molecular Sampling at Logarithmic Rates for Next-Generation Sequencing

PLoS Computational Biology

Molecular Neuroscience

English

The Position of Targeted Next-Generation Sequencing in Epidermolysis Bullosa Diagnosis

Acta Dermato-Venereologica

Dermatology

Medicine

2018

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Oliver Bartsch

Targeted Next-Generation Sequencing Analysis in Couples at Increased Risk for Autosomal Recessive Disorders

Confirmation of EP300 Gene Mutations as a Rare Cause of Rubinstein–Taybi Syndrome

Related publications

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

Autosomal Recessive Congenital Ichthyosis: CERS3 Mutations Identified by a Next Generation Sequencing Panel Targeting Ichthyosis Genes

Targeted Therapy According to Next Generation Sequencing-Based Panel Sequencing

Lessons From Next-Generation Sequencing in Genetic Skeletal Disorders

Targeted Sequencing of Cancer-Associated Genes in Hepatocellular Carcinoma Using Next Generation Sequencing

Mutation Analysis of Nine Chordoma Specimens by Targeted Next-Generation Cancer Panel Sequencing

Incidental Diagnosis of a Parental Balanced Reciprocal Rearrangement in Couples Undergoing Routine Aneuploidy Screening by Targeted Next Generation Sequencing (TNGS)

Molecular Sampling at Logarithmic Rates for Next-Generation Sequencing

The Position of Targeted Next-Generation Sequencing in Epidermo­lysis Bullosa Diagnosis

The Position of Targeted Next-Generation Sequencing in Epidermolysis Bullosa Diagnosis