Search Results - Ali Homaei

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    Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    Published 2023
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  2. 2
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    Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    Published 2022
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    Causes of Precocious Puberty in Children Referred to an Endocrine Clinic in Qazvin City, Iran From 2006 to 2018 by Fatemeh Saffari, Roghayeh Golmohammadi, Ali Homaei

    Published 2021
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    Prevalence of Sensorineural Hearing Loss in Patients with Congenital Hypothyroidism in Qazvin, Iran (2015) by Fatemeh Saffari, Mohammad Hassan Nikpendar, Neda Esmailzadehha, Sonia Oveisi, Ali Homaei, Shabnam Jalilolghadr

    Published 2018
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