Showing results 1 to 8 of 8
Title | Author(s) | Issue Date | |
---|---|---|---|
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 | ||
2018 | |||
2016 | |||
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research | 2022 | ||
2016 | |||
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 |