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Genodermatoses
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241	The Progeria Handbook A Guide for Families & Health Care Providers of Children with Progeria The mission of The Progeria Research Foundation is to discover the cause, treatment, and cure for Hutchinson-Gilford Progeria S Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:20:00 Gerontology Genodermatoses Progeria LMNA Laminopathy Progerin Jonathan Hutchinson Senescence Health Medicine Aging
242	PDF Document Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Aging Genodermatoses Gerontology Progeria Photophobia Keratitis Eyelid Sunglasses Health Medicine Ophthalmology
243	What is Prader-Willi Syndrome? Prader-Willi syndrome (PWS) is a genetic condition that affects males and females of all racial and ethnic backgrounds. It causes problems with a child’s health, behavior and learning. PW Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:12:04 Prader–Willi syndrome Hypotonia Scoliosis Health Genodermatoses Syndromes
244	THE PROGERIA SYNDROME FACT SHEET Add to Reading List Source URL: www.progeriaresearch.org Language: English - Date: 2013-08-03 16:08:00 Health Aging Gerontology Progeria Farnesyltransferase inhibitor Prenylation Progerin LMNA Farnesyltransferase Biology Genodermatoses Medicine
245	PDF Document Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Aging Gerontology Rare diseases Progeria Syndromes LMNA Progerin Laminopathy Senescence Health Medicine Genodermatoses
246	Microsoft Word - 2007DATABASECOVER _2_.DOC Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Aging Gerontology Medicine Progeria Health Genodermatoses Rare diseases
247	PDF Document Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Genodermatoses Rare diseases Stroke Aging Progeria Aspirin Ischemia Transient ischemic attack Infarction Medicine Health Aging-associated diseases
248	Microsoft Word - 2007Nov 8INFO DIAGNOSTICSTOPARENTS _2_.DOC Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Genodermatoses Rare diseases Aging Gerontology Progeria LMNA Genetic testing Point mutation Mutation Health Medicine Biology
249	Am. J. Hum. Genet. 64:1305–1315, 1999 Comprehensive Mutation Analysis of TSC1 and TSC2—and Phenotypic Correlations in 150 Families with Tuberous Sclerosis Alistair C. Jones, Magitha M. Shyamsundar, Meinir W. Thomas, Add to Reading List Source URL: www.lamhealthproject.org Language: English - Date: 2013-04-01 18:39:16 Mutation Genodermatoses Tuberous sclerosis TSC1 Angiomyolipoma TSC2 Microsatellite Point mutation Frameshift mutation Biology Genetics Medicine
250	The Progeria Handbook A Guide for Families & Health Care Providers of Children with Progeria The mission of The Progeria Research Foundation is to discover the cause, treatment, and cure for Hutchinson-Gilford Progeria S Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:02:00 Aging Gerontology Progeria Medicine CVS Caremark Genodermatoses Rare diseases Health

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