Novel non-identical MECP2 mutations in Rett syndrome family : A rare presentation
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概要
- 論文の詳細を見る
- 2012-01-01
著者
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Gulati Sheffali
Department Of Pediatrics All India Institute Of Medical Science
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Kalra Veena
Department Of Pediatrics All India Institute Of Medical Science
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GHOSH Manju
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences
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KHAJURIA Rajni
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences
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GUPTA Neerja
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences
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SAPRA Savita
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences
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KABRA Madhulika
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences
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GULATI Sheffali
Department of Pediatrics, All India Institute of Medical Sciences
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KALRA Veena
Department of Pediatric Neurology, Indraprastha Apollo Hospital
関連論文
- Hypothalamic hamartoma, gelastic epilepsy, precocious puberty-a diffuse cerebral dysgenesis
- Renal agenesis and external iliac artery stenosis in an infant with moyamoya disease
- Novel non-identical MECP2 mutations in Rett syndrome family : A rare presentation
- 8th Asian & Oceanian Congress of Child Neurology Hotel Taj Palace, New Delhi, 7-10th October 2004
- REPORT FROM INDIA, No.2