William Dobyns to Hydrops Fetalis
This is a "connection" page, showing publications William Dobyns has written about Hydrops Fetalis.
Connection Strength
0.292
-
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan; 63(1):103624.
Score: 0.173
-
Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome. Prenat Diagn. 2013 Oct; 33(10):1010-2.
Score: 0.118