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Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.
Gangodkar P, Khadilkar V, Raghupathy P, Kumar R, Dayal AA, Dayal D, Ayyavoo A, Godbole T, Jahagirdar R, Bhat K, Gupta N, Kamalanathan S, Jagadeesh S, Ranade S, Lohiya N, Oke RL, Ganesan K, Khatod K, Agarwal M, Phadke N, Khadilkar A. Gangodkar P, et al. Among authors: khatod k. Endocrine. 2021 Jan;71(1):189-198. doi: 10.1007/s12020-020-02494-z. Epub 2020 Sep 18. Endocrine. 2021. PMID: 32948948
Use of two complementary new molecular techniques, next-generation sequencing and droplet digital PCR, for diagnosis of an F8 gene deletion and subsequent carrier analysis in a family with haemophilia A: A Case Report.
Gangodkar P, Ranade S, Anand S, Bapat A, Khatod K, Shah P, Agarwal M, Phadke N. Gangodkar P, et al. Among authors: khatod k. Haemophilia. 2018 Nov;24(6):e425-e427. doi: 10.1111/hae.13613. Epub 2018 Oct 9. Haemophilia. 2018. PMID: 30299569 No abstract available.
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