Last Updated: 09/26/2026
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Found 8 publications
A Critical Assessment of Antenatal Monitoring for Fetal Well-Being in Down Syndrome Pregnancies.
Journal: Diagnostics (Basel, Switzerland)
Published: November 20, 2025
Prenatal phenotype of 47, XXY (Klinefelter syndrome).
Journal: Prenatal diagnosis
Published: July 26, 2021
Outcomes of both complex and isolated cases of infants with large stomach on fetal ultrasound.
Journal: American journal of obstetrics & gynecology MFM
Published: September 28, 2020
The Double Bubble Sign: Duodenal Atresia and Associated Genetic Etiologies.
Journal: Fetal diagnosis and therapy
Published: September 10, 2018
Severe Neonatal Manifestations of Infantile Liver Failure Syndrome Type 1 Caused by Cytosolic Leucine-tRNA Synthetase Deficiency.
Journal: JIMD reports
Published: July 23, 2018
Prenatal ABO/RHD Genotyping: A New Paradigm to Allow for Fresh Whole Blood for Cardiopulmonary Bypass in the Immediate Newborn Period.
Journal: Fetal diagnosis and therapy
Published: December 18, 2017
Juvenile Idiopathic Arthritis Associated with Combined JP-HHT Syndrome: A Novel Phenotype Associated with a Novel Variant in SMAD4.
Journal: Journal of pediatric genetics
Published: August 24, 2017
A novel PRRT2 pathogenic variant in a family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures.
Journal: Cold Spring Harbor molecular case studies
Published: August 13, 2017
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Last Updated: 09/26/2026