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Found 30 publications

Fatal Association of Mirror and Eisenmenger Syndrome during the COVID-19 Pandemic.

Description of the molecular and clinical characteristics of the mucopolysaccharidosis type VII Iberian cohort.

Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the SLC17A5 gene.

Severe fetal anaemia caused by congenital cytomegalovirus infection.

Analysis of three families with recurrence of non-immune hydrops fetalis by trio whole exome sequencing.

A mild case of hemolytic disease of the fetus and newborn due to anti-Sc2.

Ballantyne syndrome associated with fetal cardiac rhabdomyoma: a case report.

Genotypes of thalassemia in children: an analysis of 30 417 cases.

Congenital syphilis with hydrops fetalis: report of four cases in a general referral hospital in Bogota, Colombia between 2016- 2020

Application of whole exome sequencing technology in fetuses with congenital structural abnormalities.

Reliability of visual assessment of neonatal jaundice among neonates of black descent: a cross-sectional study from Tanzania.

Pattern of serum bilirubin changes following double volume exchange blood transfusion in neonates at a tertiary health facility in Nigeria.

Showing 1-12 of 30