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	1.	Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype. [electronic resource] by Narayanan, Dhanya Lakshmi Ranganath, Prajnya Balakrishnan, Surya Dalal, Ashwin Producer: 20200204 In: Clinical dysmorphology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism. [electronic resource] by Vineeth, Venugopal S Das Bhowmik, Aneek Balakrishnan, Surya Dalal, Ashwin Aggarwal, Shagun Producer: 20190321 In: Journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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