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Genodermatoses
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#	Item
11	FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang Jab Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2011-10-31 13:35:56 Anatomy Genodermatoses Tyrosine kinase receptors Fibroblast growth factor receptor 2 Apert syndrome Crouzon syndrome Craniosynostosis Fibroblast growth factor Neurocranium Health Biology Syndromes
12	Microsoft Word - Paper755u Add to Reading List Source URL: impactaging.com Language: English Proteins Genodermatoses Collagen Integrins Rare diseases Filaggrin S100A7 Wrinkle Epidermolysis bullosa Biology Anatomy Keratins
13	THE NATIONAL MEDICAL JOURNAL OF INDIA VOL. 27, NO. 5, Add to Reading List Source URL: www.nmji.in Language: English - Date: 2015-05-28 07:54:08 Ichthyosis Chronic myelogenous leukemia Melanonychia Nail disease Anonychia Genodermatoses Health Medicine
14	Brain phenotypes in two FGFR2 mouse models for Apert syndrome Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2010-02-16 13:17:22 Biology Genodermatoses Apert syndrome Craniosynostosis Fibroblast growth factor receptor 2 Corpus callosum Suture Ventriculomegaly Health Anatomy Syndromes
15	DEVELOPMENTAL DYNAMICS 239:3058–3071, 2010 a PATTERNS & PHENOTYPES Add to Reading List Source URL: www.getahead.psu.edu Language: English - Date: 2010-10-27 13:48:41 Syndromes Congenital disorders Skull Genodermatoses Craniosynostosis Apert syndrome Fibroblast growth factor receptor 2 Saethre-Chotzen syndrome Suture Health Anatomy Human anatomy
16	Table: Identified primary aetiologies that may cause deafblindness Aetiology Aetiology Hereditary/Chromosomal Syndromes and Disorders 101 Aicardi syndrome 132 Moebius syndrome Add to Reading List Source URL: www.deafblindindicators.eu Language: English - Date: 2015-03-31 17:26:31 Genodermatoses Klippel–Feil syndrome Down syndrome Klippel–Trénaunay–Weber syndrome Klippel Dandy–Walker syndrome Aicardi syndrome Chromosome 5 ICD-10 Chapter XVII: Congenital malformations deformations and chromosomal abnormalities Health Rare diseases Syndromes
17	We would like to recognize and thank our 2012 sponsors: Title Sponsor Robert McCarthy Platinum Sponsors West Liberty Beer & Tobacco Add to Reading List Source URL: www.iamcam.org Language: English - Date: 2013-06-17 21:04:46 Health Aging Gerontology Progeria Human behavior Progerin Sponsor Golf Leisure Genodermatoses Rare diseases
18	Timeline Highlights through July 2014: Our History, Our Future… March 1999: The Progeria Research Foundation (PRF) is incorporated as a Massachusetts non-profit organization. June 9, 1999: the Board of Director Add to Reading List Source URL: www.progeriaresearch.org Language: English - Date: 2014-11-10 08:11:46 Chemistry Rare diseases Aging Gerontology Progeria Lonafarnib Sirolimus Clinical trial Health Medicine Genodermatoses
19	Studies Supported and Ensuing PublicationsStudies supported - 21 Studies supported sinceStudies pending Total publications – 22 Total Studies Supported 9.11 Add to Reading List Source URL: depts.washington.edu Language: English - Date: 2013-04-17 14:46:39 Genetic genealogy Medical genetics Ichthyosis Congenital ichthyosiform erythroderma Netherton syndrome Lamellar ichthyosis X-linked ichthyosis Epidermolytic hyperkeratosis Pachyonychia congenita Genodermatoses Health Rare diseases
20	e u r o p e a n j o u r n a l o f p a e d i a t r i c n e u r o l o g y x x xe5 Official Journal of the European Paediatric Neurology Society Original article Add to Reading List Source URL: www.stsn.nl Language: English - Date: 2014-10-18 21:23:31 Health Immunosuppressants Macrolides Genodermatoses Tuberous sclerosis Everolimus Sirolimus Astrocytoma Glioma Medicine Brain tumor Biology