Majid Fardaei and Mohammad Miryounesi - Free people check

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Leigh syndrome associated with a novel mutation in the ...

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by M Miryounesi · · Cited by 11 — Mohammad Miryounesi, Majid Fardaei, Seyed Mohammadbagher Tabei and Soudeh Ghafouri-Fard. From the journal Journal of Pediatric Endocrinology ... › doi › jpem › html

Leigh syndrome associated with a novel mutation ProQuest

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by M Miryounesi · · Cited by 11 — Mohammad Miryounesi, Majid Fardaei, Seyed Mohammadbagher Tabei and Soudeh Ghafouri-Fard*. Leigh syndrome associated with a novel mutation in the COX15 gene. › openview › 1.pdf

A case report: Autosomal recessive microcephaly caused by a novel...

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Majid Fardaei b, Milad Gholami a, Mohammad Miryounesi ca Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran;

A Case Report with a Mutation in TRIOBP Gene - PubMed

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by M Fardaei · · Cited by 9 — Authors. Majid Fardaei , Shaghayegh Sarrafzadeh , Soudeh Ghafouri-Fard , Mohammad Miryounesi. Affiliations. 1 Department of Medical Genetics, ... by SK Alashti · — Authors. Shayan Khalili Alashti , Jafar Fallahi , Arezoo Jokar , Majid Fardaei. Affiliations. 1 Department of Medical Genetics, Shiraz University of Medical ... › ...

All web results to the name "Majid Fardaei"

A new missense mutation in the BCKDHB gene causes the classic form of...

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Mohammad Miryounesi, Soudeh Ghafouri-Fard, Hamedreza Goodarzi, Majid Fardaei. Journal of Pediatric Endocrinology & Metabolism: JPEM ...

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a...

ijmcmed.org

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene · Majid Fardaei 1, Shaghayegh Sarrafzadeh 2, Soudeh Ghafouri-Fard *3, Mohammad Miryounesi Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran., Department of Medical Genetics, ...

An immunocompetent patient with a nonsense Cureuswww.cureus.com › pmc_articles

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... Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi ...

A New Mutation in WT1 Gene Associated with Wilms Tumor ...

brieflands.com

Majid Fardaei , avatar Seyed Mohammad Bagher Tabei , avatar Soudeh Ghafouri-Fard ORCID , avatar Mohammad Miryounesi. 1 Department of Medical Genetics, ... › ijcm › articles

CrossRef TDM - Annals of Rehabilitation Medicine

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Mohammad Miryounesi, Seyed Mohammad Bagher Tabei, Mehdi Dianatpour, Majid Fardaei, Soudeh Ghafouri-Fard. Meta Gene ;16: Crossref logo. › journal › crossRefTDM

Leigh syndrome associated with a novel mutation in the COX15 gene :...

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Mohammad Miryounesi, Majid Fardaei, Seyed Mohammadbagher Tabei and Soudeh Ghafouri-Fard*. Leigh syndrome associated with a novel mutation in the COX15 gene. DOI jpem Received October 5, 2015; accepted January 4, 2016; previously published online March 9, Abstract: Leigh ...

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Majid Fardaei and Mohammad Miryounesi Free People Check