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Congenital ichthyosiform erythroderma
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1	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
2	Citation: Cell Death and Disease[removed], e416; doi:[removed]cddis[removed] & 2012 Macmillan Publishers Limited All rights reserved[removed]www.nature.com/cddis Novel transglutaminase 1 mutations in patients Add to Reading List Source URL: www.nature.com Language: English Rare diseases Genetics Congenital ichthyosiform erythroderma Ichthyosis Keratinocyte transglutaminase ABCA12 Lamellar ichthyosis Point mutation Transglutaminase Genodermatoses Health Biology
3	DECEMBER[removed]ICHTHYOSIS OVERVIEW Ichthyosis is a family of disorders characterized by dry or scaly and thickened skin. “Ichthy” comes from the Greek word for fish. This condition is called Add to Reading List Source URL: niams.nih.gov Language: English - Date: 2013-05-22 13:38:02 Medical genetics Ichthyosis Lamellar ichthyosis National Institute of Arthritis and Musculoskeletal and Skin Diseases X-linked ichthyosis Congenital ichthyosiform erythroderma National Institutes of Health CHILD syndrome Ichthyosis hystrix Genodermatoses Health Medicine
4	DECEMBER[removed]ICHTHYOSIS OVERVIEW Ichthyosis is a family of disorders characterized by dry or scaly and thickened skin. “Ichthy” comes from the Greek word for fish. This condition is called Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2013-05-22 13:38:02 Medical genetics Ichthyosis Lamellar ichthyosis National Institute of Arthritis and Musculoskeletal and Skin Diseases X-linked ichthyosis Congenital ichthyosiform erythroderma National Institutes of Health CHILD syndrome Ichthyosis hystrix Genodermatoses Health Medicine
5	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Biology Rare diseases Dorfman Histopathology Neutral lipid storage disease Hepatitis Hepatology Congenital ichthyosiform erythroderma Cirrhosis Health Medicine Genodermatoses