Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 1 (of 1 Records)

Query Trace: Ellis-Van Creveld Syndrome and WDR35[original query]
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.
Clinical genetics 2017 9 93 (3): 632-639.
Niceta M, Margiotti K, Digilio M C, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici M L, Consoli F, Torrente I, Ruiz-Perez V L, Dallapiccola B, Marino B, De Luca A, Tartaglia
TOP