Coffin-Lowry Syndrome Foundation Return to Search Page coffinlowry syndrome Foundation. 3045 255th Ave SE Sammamish,WA 98075 Conditions coffin-lowry syndrome. Hours Answered after 530pm PST http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Coff
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Nature Publishing Group Practical Genetics. Xlinked coffin-lowry syndrome (CLS, MIM 303600, RPS6KA3 gene,protein product known under various names pp90 rsk2 , RSK2, ISPK, MAPKAP1). http://www.nature.com/cgi-taf/DynaPage.taf?file=/ejhg/journal/v10/n1/full/520073
Nature Publishing Group Original paper. Germline mosaicism in coffinlowry syndrome. Sylvie Keywords.coffin-lowry syndrome; RSK2 mutation; germline mosaicism. Received http://www.nature.com/cgi-taf/DynaPage.taf?file=/ejhg/journal/v6/n6/abs/5200230a
GeneReviews: Coffin-Lowry Syndrome Your browser does not support HTML frames so you must view coffinlowry Syndromein a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/cls
GeneClinics: Diseases And Overviews Central Nervous System Hypomelination/Vanishing White Matter ChoreoacanthocytosisChoroideremia Cockayne syndrome coffinlowry syndrome Congenital Contractural http://www.geneclinics.org/profiles/
ORPHANET® : Coffin-Lowry Syndrome Translate this page ORPHANET. ORPHANET database access. coffin-lowry syndrome.Direct access to details Alias Home Page. http://www.orpha.net/static/GB/coffin_lowry.html
Service Page - Pathologie Information Translate this page MALADIE coffin-lowry, syndrome de, CIM Q87.8, Le syndrome de coffin-lowry(CLS) est une maladie génétique d'expression semi-dominante http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=192
Coffin-Lowry Translate this page coffin-lowry syndrome a multicenter study. Clin Genet 1988 34 230-45. Mutationsin the kinase Rsk-2 associated with coffin-lowry syndrome. http://orphanet.infobiogen.fr/data/patho/coflowry.html
Analysis Of Coffin-Lowry Syndrome Analysis of coffinlowry syndrome, G2D Home. GO TO CHROMOSOMAL REGION Disease mappedcoffin-lowry syndrome Chromosome X Genomic position start-stop 8000001 http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U1210
Complete List Of Candidates Associated To Coffin-Lowry Syndrome Complete list of candidates associated to coffinlowry syndrome, G2DHome. The graph represents the BLASTX hits found in the region http://www.bork.embl-heidelberg.de/g2d/list_hits_disease.pl?U1210:Coffin-Lowry_s
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Extractions: Epileptic Disorders. Vol. 2, Issue 3, September 2000 Epileptic Disorders. Vol. 2, Issue 3, September 2000: 173-6, Case report Summary: We present a patient with a complete Coffin-Lowry syndrome, associated with drop episodes precipitated by sudden auditory stimuli, which provoked in turn, a definite loss of muscle tone in both legs. Electrophysiological studies showed that these episodes are an unusual type of startle response and that they may be associated with Coffin-Lowry syndrome.
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CyberSpace Search! SEARCH THE WEB. Results 1 through 2 of 2 for coffinlowry syndrome. http://www.cyberspace.com/cgi-bin/cs_search.cgi?Terms=coffin-lowry syndrome
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