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 - Neurofibromatosis - Document - PDFSEARCH.IO

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Date: 2011-11-02 17:53:58 Neuro-cardio-facial-cutaneous syndromes Neurological disorders Medical signs Neurofibromatosis type I Neurofibromatosis Neurofibroma Café au lait spot Lisch nodule Neurofibromin 1 Medicine Health Genodermatoses		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 Add to Reading List Source URL: www.journal-imab-bg.org Download Document from Source Website File Size: 279,99 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
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	WHAT YOU CAN DO There is a lot you can do to keep hope alive and improve the future of someone with NF. Most importantly, you can be proactive, and involved in the NF cause and community. Make a Donation DocID: GiDW - View Document