Group by: Item Type | No Grouping Jump to: Article Number of items: 2. ArticleDhanya Lakshmi, N. and Ranganath, P. and Balakrishnan, S. and Dalal, Ashwin (2019) Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype. Clinical Dysmorphology, 28 (4). pp. 202-204. ISSN 0962-8827 Vineeth, V.S. and Das Bhowmik, A. and Balakrishnan, S. and Dalal, Ashwin and Aggarwal, Shagun (2019) Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism. Journal of Human Genetics, 64 (1). pp. 183-189. ISSN 1434-5161
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