Dr. med. Axel Bohring
human genetics, pediatrics
human genetics, pediatrics
Overview
Country, City
Germany, Munster
Health facility
University Hospital Munster
Medical unit
Department of human genetics
About the doctor
Skills & Expertise
genetics
dysplasia
frontometaphyseal dysplasia
phenotype
bohringopitz syndrome
charge syndrome
ehlersdanlos syndrome
hypohidrotic ectodermal dysplasia
trigonocephaly syndrome
truncating mutations
multiple osteochondromas
vertebral column
skeletal dysplasia
polytopic anomalies
prepubertal periodontitis
nodular heterotopia
meckelgruber syndrome
capillary dysplasia
pulmonary veins
tumorigenesis mutations
schwannomatosis
alveolar capillary dysplasia
lower vertebral column
sclerosing skeletal dysplasia
sporadic familial cases
misaligned pulmonary veins
kbg syndrome
osteochondromas
immunoglobulin
pancreas
mutation
face
anomalies
deletion
sclerosing
heterozygotes
agenesis
predispose
sweating
ectodermal dysplasia
dystrophies
haplotype
periventricular
heterotopia
pregnancy loss
genetic disorders
neurofibromatosis
retinal dystrophies
waardenburg syndrome
noonan syndrome
Resume
CV (Curriculum Vitae)
Education
- Studied human medicine
- Obtaining a license for medical practice
- Obtaining specialization in pediatrics
- Received additional specialization in human genetics
Experience
- Acting director of the institute at the Westphalian Wilhelms University in Munster
- Department of human genetics at the University Hospital Munster
Languages
English
German
Publications
Location
Albert-Schweitzer-Campus, 1, 48149 Munster, Germany
FAQ
Where does the doctor practice?
What is the specialization of Dr. med. Axel Bohring?
The primary specialization of the doctor is human genetics, pediatrics.
What is the rating of the doctor?
Dr. med. Axel Bohring is rated as 9.90 by AiroMedical.
Dr. med. Axel Bohring
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