Showing 1 - 4 results of 4 for search 'Ali Homaei', query time: 0.05s Refine Results
  1. 1
    Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome

    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
    Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series

    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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  3. 3
    Causes of Precocious Puberty in Children Referred to an Endocrine Clinic in Qazvin City, Iran From 2006 to 2018

    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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  4. 4
    Prevalence of Sensorineural Hearing Loss in Patients with Congenital Hypothyroidism in Qazvin, Iran (2015)

    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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