Showing results 1 to 10 of 10
Title | Author(s) | Issue Date | |
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A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway Journal:Molecular Human Reproduction | 2016 | ||
A Practical Guide for Mapping Short Reads Book:Deep Sequencing Data Analysis | 2013 | ||
2018 | |||
2016 | |||
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research | 2022 | ||
2016 | |||
Hnrnpa1 Mutations Cause Congenital Heart Defects Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017 | 2017 | ||
Mapping of a Hirschsprung's disease locus in 3p21 Journal:European Journal of Human Genetics | 2008 | ||
Mutational analysis of SHH and GLI3 in anorectal malformations Journal:Birth Defects Research Part A - Clinical and Molecular Teratology | 2008 | ||
2011 |