Afsaneh Labbaf
发表
F. Kazerouni,
M. Omrani,
H. Ghaedi,
2017,
Journal of medical biochemistry.
Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome
H. Ghaedi,
H. Darvish,
Maryam Omidvar,
2019,
Genes & diseases.
F. Kazerouni,
M. Omrani,
H. Ghaedi,
2017,
Clinical Laboratory.