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	1.	Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex. [electronic resource] by S Suttur, Malini R Mysore, Savitha Krishnamurthy, Balasundaram B Nallur, Ramachandra Producer: 20110714 In: Indian journal of human genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A rare case of congenital heart disease with ambiguous genitalia. [electronic resource] by Lingaiah, Kusuma Parshwanath, Bharath A Mysore, Savitha R Krishnamurthy, Balasundaram Ramachandra, Nallur B Producer: 20110714 In: Indian journal of human genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Missense mutation G296S in GATA4 is not responsible for cardiac septal defects. [electronic resource] by Ramegowda, Smitha Kumar, Arun Savitha, Mysore R Krishnamurthy, Balasundaram Doddaiah, Narayanappa Ramachandra, Nallur B Producer: 20111110 In: Indian journal of human genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India. [electronic resource] by Dinesh, Sosalagere M Lingaiah, Kusuma Savitha, Mysore R Krishnamurthy, Balasundaram Narayanappa, Doddaiah Ramachandra, Nallur B Producer: 20120203 In: Genetic testing and molecular biomarkers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India. [electronic resource] by Kusuma, Lingaiah Dinesh, Sosalagere M Savitha, Mysore R Krishnamurthy, Balasundaram Narayanappa, Doddaiah Ramachandra, Nallur B Producer: 20111115 In: Genetic testing and molecular biomarkers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	De novo isochromosome 18p in a female dysmorphic child. [electronic resource] by Ramegowda, Smitha Gawde, Harshavardhan M Hyderi, Abbas Savitha, Mysore R Patel, Zareen M Krishnamurthy, Balasundaram Ramachandra, Nallur B Producer: 20070212 In: Journal of applied genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)