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X-linked mental retardation
Results: 8

#	Item
1	Coffin-Lowry Syndrome The Coffin–Lowry syndrome (CLS) (MIMis a syndromic form of X-linked mental retardation characterized in male patients by psychomotor retardation, growth retardation, and various skeletal Add to Reading List Source URL: www.ssbp.org.uk Language: English - Date: 2015-05-13 15:34:29 Genetic genealogy Medical genetics Mental retardation RPS6KA3 X-linked mental retardation Sensorineural hearing loss Rare diseases Ciliopathy Fryns Syndrome Health Syndromes Coffin–Lowry syndrome
2	SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Coffin-Lowry Syndrome Add to Reading List Source URL: www.qcidd.com.au Language: English - Date: 2013-02-13 00:06:40 Genetic genealogy Medical genetics Mental retardation RPS6KA3 X-linked mental retardation Rare diseases Ribosomal s6 kinase Sensorineural hearing loss Fryns Syndrome Health Syndromes Coffin–Lowry syndrome
3	The Genetics of Rett Syndrome John Christodoulou Head, NSW Rett Syndrome Research Unit Western Sydney Genetics Program, Children’s Hospital at Westmead Discipline of Paediatrics & Child Health, University of Sydney Add to Reading List Source URL: www.apsu.org.au Language: English - Date: 2012-12-20 21:53:57 Autism Transcription factors Genes MECP2 Syndromes Rett syndrome X-linked mental retardation Mutation Epigenetics Genetics Biology Health
4	Structural, Dynamical and Energetical Consequences of Rett Syndrome Mutation R133C in MeCP2 Tugba G Kucukkal, Emil Alexov Computational Biophysics and Bioinformatics, Department of Physics, Clemson University, Clemson, Add to Reading List Source URL: downloads.hindawi.com Language: English* - Date: 2015-03-11 18:15:01 Protein domains Protein structure Genes MECP2 Rett syndrome Root-mean-square deviation X-linked mental retardation DNA Methylation Biology Chemistry Genetics
5	Coffin–Lowry syndrome Add to Reading List Source URL: www.nature.com Language: English - Date: 2010-05-20 10:43:12 Medical genetics Coffin–Lowry syndrome Mental retardation Genodermatoses RPS6KA3 Ribosomal s6 kinase X-linked mental retardation Lujan-Fryns syndrome Health Syndromes Genetic genealogy
6	Gen_Genetic_Test Genetic Test Subjectkey (NDAR GUID) Source subject ID Age (in months) Genetic test Add to Reading List Source URL: ndar.nih.gov Language: English - Date: 2014-11-20 22:13:46 Biology PHF8 1q21.1 deletion syndrome 3q29 microdeletion syndrome 22q13 deletion syndrome Fragile X syndrome MECP2 FMR1 X-linked mental retardation Health Syndromes Genetics
7	INTEGRATIVE HEALTH SCIENCES FACILITY PUBLICATIONS 2007-Present Abidi FE, Miano MG, Murray JC, Schwartz CE. A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate. Cli Add to Reading List Source URL: cph.uiowa.edu Language: English - Date: 2011-11-10 17:09:05
8	European Journal of Human Genetics[removed], 896–903 & 2006 Nature Publishing Group All rights reserved[removed] $30.00 Add to Reading List Source URL: www.nature.com Language: English - Date: 2007-02-01 05:21:44 Transcription factors Autism Syndromes Rett syndrome MECP2 CDKL5 X-linked mental retardation DNA methylation Biology Genetics Health

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