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Publications by C. de Die
OP27.03: Prenatal Diagnosis of MOPD Type I Caused by Mutations in the RNU4ATAC Gene: A Case Report
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
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Prenatal Diagnosis of Achondrogenesis Type I: A Case Report
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Mitochondrial Diseases Caused by Mutations of the POLG Gene: Problems of Differential Diagnosis
PERINATOLOGIYA I PEDIATRIYA
EP06.26: Prenatal Diagnosis of Achondroplasia: Case Report
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
A Human Immunodeficiency Caused by Mutations in the PIK3R1 Gene
Journal of Clinical Investigation
Medicine
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I
Science
Multidisciplinary
Philosophy of Science
History
EP11.18: Prenatal Diagnosis of Amniotic Band Syndrome: A Case Report
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
Prenatal Diagnosis of Klippel-Trenaunay-Weber Syndrome: A Case Report
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
Type I Renal Tubular Acidosis Caused by Sjögren’s Syndrome With Hypokalemia as the First Symptom: A Case Report
Journal of International Medical Research
Biochemistry
Medicine
Cell Biology
Prenatal Diagnosis of a Giant Fetal Cervical Teratoma by Magnetic Resonance Imaging: A Case Report
Medical Science and Discovery
