Search Results - "Thalla, Maunika"

Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism by Kollati, Yedukondalu, Akella, Radha Rama Devi, Naushad, Shaik Mohammad, Borkar, Divya, Thalla, Maunika, Nagalingam, Swapna, Lingappa, Lokesh, Patel, Rajesh K., Reddy, G. Bhanuprakash, Dirisala, Vijaya R.

“…High prevalence of congenital hypothyroidism (CH) among Indian newborns prompted us to establish population-specific reference ranges of TSH and to explore the…”
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The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism by Kollati, Yedukondalu, Akella, Radha Rama Devi, Naushad, Shaik Mohammad, Thalla, Maunika, Reddy, G Bhanuprakash, Dirisala, Vijaya R.

“…The objective of the current study is to explore the association of thyroid-stimulating hormone receptor ( TSHR ) rs1991517 polymorphism (c.2337 C > G,…”
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