Publications
Export 2 results:
Author Title [ Year
] Filters: Author is Leal, Suzanne M and Keyword is Multifactorial Inheritance [Clear All Filters]
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Med Genet 19, 122 (2018).
Variant association tools for quality control and analysis of large-scale sequence and genotyping array data. Am J Hum Genet 94, 770-83 (2014).
