Upload Records Snowball Search Search OpenAlex
About the database ScholarIQanswers from OpenAlex
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
PaperCitations, authors & open-access status
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 300 citations, 1996 year and green oa status.
300
Citations
1996
Year
green
OA Status