BRAND MANUAL_MODIFICATO-TRACC

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Neurological disorders Stroke Moyamoya disease Genodermatoses Neuro-cardio-facial-cutaneous syndromes Neurofibroma NF1 Neurofibromin 1 Chromosome 17 Medicine Health Cerebrovascular diseases		BRAND MANUAL_MODIFICATO-TRACC Add to Reading List Source URL: www.ijponline.net Download Document from Source Website File Size: 1.006,75 KB Share Document on Facebook

	Neurofibromatosis Type 1 (NF1) Genetics Autosomal dominant. Gene localised to 17q11.2. The gene product (neurofibromin) is thought to suppress tumour formation by regulating cell division. A high spontaneous mutation rat DocID: 19X22 - View Document
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	DOI: jimabJournal of IMAB - Annual Proceeding (Scientific Papers) 2008, vol. 14, book 1 A CASE OF NEUROFIBROMATOSIS TYPE 1 Valentina Dimitrova1, Ivelina Yordanova1, Verka Pavlova1, Valentin Valtchev DocID: 14xuv - View Document
	SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Neurofibromatosis Type 1 (NF1) DocID: 14vAA - View Document
	New BRAF knock-in mice provide a pathogenetic mechanism of developmental defects and a therapeutic approach in cardio-facio-cutaneous syndrome Associate Professor AOKI, Yoko Dr. Yoko Aoki’s research group has been stud DocID: 11w2F - View Document