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Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling.
Narayanan DL, Udyawar D, Kaur P, Sharma S, Suresh N, Nampoothiri S, do Rosario MC, Somashekar PH, Rao LP, Kausthubham N, Majethia P, Pande S, Ramesh Bhat Y, Shrikiran A, Bielas S, Girisha KM, Shukla A. Narayanan DL, et al. Among authors: somashekar ph. Eur J Hum Genet. 2021 Dec;29(12):1774-1780. doi: 10.1038/s41431-021-00933-7. Epub 2021 Jul 19. Eur J Hum Genet. 2021. PMID: 34276053 Free PMC article.
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