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 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](https://www.pdfsearch.io/img/7ce3e4709049a4fcc11d12a1b890687a.jpg) | Add to Reading ListSource URL: www.ssbp.org.ukLanguage: English - Date: 2015-05-13 15:34:29
|
---|
2![SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Coffin-Lowry Syndrome SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Coffin-Lowry Syndrome](https://www.pdfsearch.io/img/4b44c7e2912c0fa37db0e78d21e61fb8.jpg) | Add to Reading ListSource URL: www.qcidd.com.auLanguage: English - Date: 2013-02-13 00:06:40
|
---|
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 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](https://www.pdfsearch.io/img/6d1129a4b5ff5dd895303b17a67dc595.jpg) | Add to Reading ListSource URL: www.apsu.org.auLanguage: English - Date: 2012-12-20 21:53:57
|
---|
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, 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,](https://www.pdfsearch.io/img/e88c8be2d23c111be4a4b63349f5a6b0.jpg) | Add to Reading ListSource URL: downloads.hindawi.comLanguage: English - Date: 2015-03-11 18:15:01
|
---|
5![Coffin–Lowry syndrome Coffin–Lowry syndrome](https://www.pdfsearch.io/img/847b501acea49d9f0febafe349dfe8b6.jpg) | Add to Reading ListSource URL: www.nature.comLanguage: English - Date: 2010-05-20 10:43:12
|
---|
6![Gen_Genetic_Test Genetic Test Subjectkey (NDAR GUID) Source subject ID Age (in months) Genetic test Gen_Genetic_Test Genetic Test Subjectkey (NDAR GUID) Source subject ID Age (in months) Genetic test](https://www.pdfsearch.io/img/2c89472108b9ff2da0bcae8479a71fbf.jpg) | Add to Reading ListSource URL: ndar.nih.govLanguage: English - Date: 2014-11-20 22:13:46
|
---|
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 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](https://www.pdfsearch.io/img/f3e03a9e4766415f2f6f8e0b09a9cc4b.jpg) | Add to Reading ListSource URL: cph.uiowa.eduLanguage: 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 European Journal of Human Genetics[removed], 896–903 & 2006 Nature Publishing Group All rights reserved[removed] $30.00](https://www.pdfsearch.io/img/2e875df7aab641f49d26aac599988abc.jpg) | Add to Reading ListSource URL: www.nature.comLanguage: English - Date: 2007-02-01 05:21:44
|
---|