Associate Professor, Pediatrics, UC, Davis School of Medicine
Medical Genetics
Dr. Billur Moghaddam, MD
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Billur Moghaddam practices Medical Genetics. Billur Moghaddam, MD is also a published doctor. She has 7 publication published. The most recent publication is: Recurrent HERV-H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays.
Publications
- Recurrent HERV-H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays.
- Minor physical anomalies in children with autism spectrum disorders.
- Monosomy 21q22.11-q22.13 presenting as a Fanconi anemia phenotype.
- A novel mutation in a Fijian boy with Shwachman-Diamond syndrome.
- Floating-Harbor syndrome and intramedullary spinal cord ganglioglioma: case report and observations from the literature.
- Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Schools
Istanbul Universitesi Cerrahpasa Tip Fakultesi
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
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Washington University -
Istanbul University Faculty of Medicine
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