Baylor Hopkins Center for Mendelian Genomics (BH CMG)

Study ID Alternative Stable ID Type
phs000711 Mixed

Study Description

The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underlie Mendelian conditions. By discovering genes that cause Mendelian conditions, we will expand our understanding of their biology to facilitate diagnosis and new treatments.

Archive Link Archive Accession
dbGaP phs000711

Who archives the data?

There are no publications available