Customize your search results with filters

Term Search
You can select from the dropdown list OR enter your own terms to refine the search.
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 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.

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

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

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.

Tale of two viruses: parvovirus B19 and HIV.

Non-immune hydrops fetalis secondary to congenital chylothorax with diffuse interstitial lung disease: a diagnostic conundrum.

Showing 1-12 of 21