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Fatemeh Pourfatemi
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Fatemeh Pourfatemi
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Fatemeh Pourfatemi
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1
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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Article
2
Screening of Autosomal Recessive Non-Syndromic Hearing Loss gor GJB2 Mutations
by
Atefeh Khosh-Aeen
,
Fatemeh
Pourfatemi
,
Kimia Kahrizi
,
Yaser Riaz-Alhosseini
,
Marziyeh Mohseni
,
Niloufar Bazzaz-Zadegan
,
Nooshin Nik-Zaat
,
Hossein Najm-Abadi
Published 2004-06-01
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