Peter Meyer

发表

BRCA2 Mutations and Triple-Negative Breast Cancer

W. Eiermann, B. Ataseven, B. Högel, 2012, PloS one.

Targeted next-generation sequencing analysis in couples at increased risk for autosomal recessive disorders

S. Schweiger, J. Winter, U. Zechner, 2018, Orphanet Journal of Rare Diseases.

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

Pascal Borry, Heidi C Howard, Jörg Schmidtke, 2014, European Journal of Human Genetics.

EMQN Best Practice Guidelines for Molecular Genetic Analysis in Hereditary Breast/Ovarian Cancer

Å. Borg, N. Loman, C. Lázaro, 2008 .