Novel MEN 1 gene findings in rare sporadic insulinoma—a case control study

by Jyotsna, Viveka P., Malik, Ekta, Birla, Shweta, Sharma, Arundhati
Published 2015

Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation

by Birla, Shweta, Singla, Rajiv, Sharma, Arundhati, Tandon, Nikhil
Published 2014

Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation

by Birla, Shweta, Aggarwal, Sameer, Sharma, Arundhati, Tandon, Nikhil
Published 2014

Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency

by Birla, Shweta, Jyotsana, P Vieveka, Sharma, Arundhati, Khadgawat, Rajesh, Garg, MK, Jain, Vandana
Published 2012

Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families

by Yadav, Sarita, Birla, Shweta, Marumudi, Eunice, Sharma, Arundhati, Khadgawat, Rajesh, Khurana, M. L., Ammini, A. C.
Published 2015

Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma

by Birla, Shweta, P Jyotsna, Viveka, Singla, Rajiv, Tripathi, Madhavi, Sharma, Arundhati
Published 2015