9 results on '"Srivastava, Anand K."'
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2. Differential diagnosis of Smith–Magenis syndrome: 1p36 deletion syndrome
3. Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3
4. From ectodermal dysplasia to selective tooth agenesis
5. Evidence thatSIZN1is a candidate X-linked mental retardation gene
6. Sequence variants within exon 1 of MECP2 occur in females with mental retardation. Am J Medical Genetics Part B (Neuropsychiatric Genetic) 144B:355–360 (2007)
7. AGTR2 in brain development and function
8. A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia
9. POMGnT1 gene alterations in a family with neurological abnormalities
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