Defects » Other
- A case of a giant chorioangioma
- A case of amniotic band syndrome
- A case of herlequin fetus, ichthyosis congenita
- A case of I Cell disease
- A case of neonatal genital prolapse
- A case of persistent right umblical vein
- A case of phocomelia associated with diaphragmatic hernia
- Anomalous origin of a Shepherd Hook ductus arteriosus: an obstructive kink should be of concern
- Antepartum transabdominal amnioinfusion in idiopathic oligohydramnios
- Association between 1p36 copy number variations, abnormal expression of PEX10 gene and epilepsy phenotype
- Contemporary management of fetal anemia due to red cell alloimmunisation: factors affecting perinatal outcome
- Diagnostic algorithm and protocol for the management of fetal ascites
- Effects of abdominal decompression on fetal umbilical artery and middle cerebral artery blood flow
- Fetal abnormalities associated with single umbilical artery and genetic counselling
- Hydrops fetalis with deletion of macro domain containing 2
- Immunomodulatory effects of umbilical cord-derived mesenchymal stem cells
- Magnetic resonance imagingT1 relaxation properties of fetal blood in normal fetuses and fetuses suspected of anemia
- Molecular genetic analysis of 3 patients featuring mental retardation and developmental delay
- Nonimmune Hydrops Fetalis: Ultrasound diagnosis in patients with systemic autoimmune diseases
- Placental chorioangioma and fetal hepatic hemangioma coexistence causing fetal high-output heart failure
- Prenatal diagnosis of duplication cyst of the tongue
- Prenatal diagnosis of primary immunodeficiency: an emerging experience in Egypt
- Prenatal features of neurofibromatosis type 1
- Recurrent pregnancy loss due to hydrops fetalis caused by alpha thalassemia
- Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy