Katharina Schoner
Marburg An Der Lahn, HE, Germany
Last Updated: 09/26/2026
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Found 20 publications
Case Report: Pregnant ROS1+ lung cancer patient treated with crizotinib - Impact on infancy.
Journal: Frontiers in oncology
Published: January 10, 2026
Intrapericardial Teratoma and Associated 3q29 Deletion in a Fetus: Case Report.
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: August 20, 2024
Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one case.
Journal: Orphanet journal of rare diseases
Published: November 06, 2023
The Complexity of SARS-CoV-2 Infection in the Clinical Setting of Obstetrics - Discussion Based on a Case Study
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: September 01, 2022
Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations.
Journal: Orphanet journal of rare diseases
Published: July 08, 2022
Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain.
Journal: European journal of human genetics : EJHG
Published: July 22, 2021
Compound Heterozygous Frameshift Mutations in MESD Cause a Lethal Syndrome Suggestive of Osteogenesis Imperfecta Type XX.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: November 03, 2020
Correction: The genomic and clinical landscape of fetal akinesia.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 27, 2020
Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.
Journal: Birth defects research
Published: August 23, 2019
The genomic and clinical landscape of fetal akinesia.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 29, 2019
Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.
Journal: JCI insight
Published: September 07, 2018
Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.
Journal: American journal of medical genetics. Part A
Published: November 16, 2017
Last Updated: 09/26/2026