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Number of items: 4.

Bhat, V and Girimaji, SC and Mohan, G and Arvinda, HR and Singhmar, P and Duvvari, MR and Kumar, A (2011) Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations. In: Clinical Genetics, 80 (6). pp. 532-540.

Kumar, A and Blanton, SH and Babu, M and Markandaya, M and Girimaji, SC (2004) Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations. In: Clinical Genetics, 66 (4). pp. 341-348.

Savithri, HS and Murthy, Venkatesha Hs and Baskaran, G and Rao, Appaji N and Kool, D and Edkins, E and Wang, W and Bittles, AH (2000) Predictive testing for familial adenomatous polyposis in a rural South Indian community. In: Clinical Genetics, 58 (1). pp. 57-60.

Rao, Appaji N and Devi, Radha Rama A and Savithri, HS and Rao, Venkat S and Bittles, AH (1988) Neonatal screening for amino acidaemias in Karnataka, south India. In: Clinical Genetics, 34 (1). pp. 60-63.

This list was generated on Tue Jul 5 21:37:03 2022 IST.