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Genetics Neuro-cardio-facial-cutaneous syndromes Syndromes Neurofibromatosis type I Watson syndrome Neurofibromatosis Neurofibroma Noonan syndrome Lisch nodule Medicine Health Genodermatoses		Add to Reading List Source URL: jmg.bmj.com Download Document from Source Website File Size: 645,82 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
	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
	Peripheral Nerve Tumors ________________________________________________ Johns Hopkins AJB/13 DocID: FkRL - View Document
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