Hasil Pencarian - Priyanshu Mathur

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  1. 1
    Hypohydrotic ectodermal dysplasia: A rare case series

    Hypohydrotic ectodermal dysplasia: A rare case series oleh Manisha Goyal, Ashok Gupta, Priyanshu Mathur, Manish Sharma

    Diterbitkan 2018-01-01
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  2. 2
    A case of cervicomedullary junction compression

    A case of cervicomedullary junction compression oleh Ashok Gupta, Priyanshu Mathur, Manish Sharma, Vimesh Parmar

    Diterbitkan 2017-01-01
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  3. 3
    Fetal Valproate Syndrome with Limb Defects: An Indian Case Report

    Fetal Valproate Syndrome with Limb Defects: An Indian Case Report oleh Manisha Goyal, Ashok Gupta, Manish Sharma, Priyanshu Mathur, Naresh Bansal

    Diterbitkan 2016-01-01
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  4. 4
    A case of Landau-Kleffner syndrome

    A case of Landau-Kleffner syndrome oleh Manjunath S Pandit, Ashok Gupta, Priyanshu Mathur, Manish Sharma, Manisha Garg

    Diterbitkan 2016-01-01
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  5. 5
    A rare case of wegeners granulomatosis with allergic bronchopulmonary aspergillosis in a child

    A rare case of wegeners granulomatosis with allergic bronchopulmonary aspergillosis in a child oleh Vikas Gupta, Ashok Gupta, Priyanshu Mathur, Manish Sharma, Manisha Garg, Rajesh Kumar

    Diterbitkan 2016-01-01
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  6. 6
    Oro facial digital syndrome type 2- An Indian case report

    Oro facial digital syndrome type 2- An Indian case report oleh Naresh Bansal, Ashok Gupta, Manisha Goyal, Manish Sharma, Priyanshu Mathur, Manish Agarwal

    Diterbitkan 2016-01-01
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  7. 7
    A rare case of glycogen storage disease type XI fanconi-bickel syndrome

    A rare case of glycogen storage disease type XI fanconi-bickel syndrome oleh Manisha Garg, Ashok Gupta, Priyanshu Mathur, Manish Sharma, Rajesh Kumar, Vikas Gupta, M Manjunath

    Diterbitkan 2016-01-01
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