Rezultati pretrage - Shruti Bajaj

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  1. 1
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    Recurrent variant c.1680C>A in FAM20C gene and genotype-phenotype correlation in a patient with Raine syndrome: a case report od Shruti Bajaj, Fazal Nabi, Jhanvi Shah, Harsh Sheth

    Izdano 2021
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  2. 2
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    An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case report od Shruti Bajaj, Purnima Satoskar, Aadhira Nair, Frenny Sheth, Jayesh Sheth, Harsh Sheth

    Izdano 2022
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