Katharina M. Roetzer
Vienna, Austria
Last Updated: 09/26/2026
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Found 9 publications
Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.
Journal: European journal of human genetics : EJHG
Published: October 14, 2025
Genetic counselling legislation and practice in cancer in EU Member States.
Journal: European journal of public health
Published: June 21, 2024
Identifying adult hypophosphatasia in the rheumatology unit.
Journal: Orphanet journal of rare diseases
Published: March 16, 2022
Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH).
Journal: Journal of structural biology
Published: March 01, 2020
Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization.
Journal: Bone
Published: October 11, 2017
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.
Journal: American journal of human genetics
Published: May 10, 2017
A child with split-hand/foot associated with tibial hemimelia (SHFLD syndrome) and thrombocytopenia maps to chromosome region 17p13.3.
Journal: American journal of medical genetics. Part A
Published: October 11, 2013
Re-alignment-procedures for skeletal dysplasia in three patients with genetically diverse syndromes.
Re-alignment-procedures for skeletal dysplasia in three patients with genetically diverse syndromes.
Journal: Orthopaedic surgery
Published: June 05, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026