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Samira Molaei Ramsheh
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Samira Molaei Ramsheh
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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome
by
Hamid Ghaedi
,
Samira
Molaei
Ramsheh
,
Maryam Erfanian Omidvar
,
Afsaneh Labbaf
,
Elham Alehabib
,
Sanaz Akbari
,
Fatemeh Pourfatemi
,
Hossein Darvish
Published 2020-12-01
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