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Biochemical studies on handigudu disease : a familial syndrome of EPI(META) Physeal dysplasia.

By: Mallikarjun BadadaniMaterial type: Text

TextSeries: ; Publication details: Bangalore Dept of Neurochemistry NIMHANS 2006Edition: Description: 200 p. 28 cmSubject(s): Dysplasia Epiphysialis Punctata | Chondrodysplasis PunctataDDC classification: A7.1 Summary: Chondrodysplasis Punctata, Dysplasia Epiphysialis Punctata

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Item type	Current library	Home library	Collection	Call number	Status	Date due	Barcode
Gift Dissertations	Library and Information Centre	Library and Information Centre Reference	Ph.D Neurochemistry	A7.1 MAL 2006 (Browse shelf (Opens below))	Available		GD3057

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Previous	A7.1 KRI 1997 Studies on biochemical mechanisms underlying neurotoxin induced damage	A7.1 KRU 2007 Study of gene polymorphisms in puerperal cerebral venous thrombosis	A7.1 LAK 1989 Biochemical and genetic studies in affective disorders	A7.1 MAL 2006 Biochemical studies on handigudu disease :	A7.1 MAM 1994 Biochemical regulation and expression of cyclic adenosine monophosphate in rat brain with special reference to neuronal function	A7.1 MAM 2011 Hyperhomocysteinemia,methylarginines and vascular endothelial,dysfernction :study in ischemic stroke	A7.1 MAT 2012 Role of insulin in alzhemimer's disease	Next

Ph.D in Neurochemistry

Chondrodysplasis Punctata, Dysplasia Epiphysialis Punctata

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