Search Results - Mohammad KERAMATIPOUR

Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene by Mona ENTEZA­M, Akbar AMIRFIROOZI, Mansoureh TOGHA, Mohammad KERAMATIPOUR

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Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

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PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data by Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour

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Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone by Mohammad Keramatipour, Babak Ahadi, Mohsen Taghizadeh, Ali Tabibi, Farshad Zohrabi, Babak Javanmard, Behzad Narouie

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Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

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Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report by Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR

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Setting up Multiplex Panels for Genetic Testing of Familial Hypertrophic Cardiomyopathy Based on Linkage Analysis by Hoorieh SAGHAFI, Majid HAGHJOO, Sima SABBAGH, Niloofar SAMIEE, Farve VAKILIAN, Mohammad TAGHI SALEHI OMRAN, Masoomeh DADASHI, Ahmad AMIN, Mohammad KERAMATIPOUR

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