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Coffin Lowry Syndrome: more detail

The Official Parent's Sourcebook on Coffin-lowry Syndrome: A Directory for the Internet Age by Icon Health Publications, 2005-01-30

Coffin-Lowry Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20

Coffin-Lowry syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Roger, MD Stevenson, 2005

lists with details

1Up Health > Coffin-Lowry Syndrome - Birth Defects & Genetic Disorders
CoffinLowry Syndrome . Read detailed information about Coffin-Lowry Syndrome. Main Article. What is coffin lowry syndrome? Is there any treatment?
http://www.1uphealth.com/medical/disease/birth-defects-genetic-disease/coffin-lo

Extractions: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory
1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders
Sites. coffin lowry syndrome Information sheet compiled by the NationalInstitute of Neurological Disorders and Stroke (NINDS). Coffin
http://www.1uphealth.com/links/genetic-disorders-coffin-lowry-syndrome.html
Coffin Lowry Syndrome
coffin lowry syndrome coffin lowry syndrome factsheet NationalInstitute for Neurological Disorders and Stroke. disclaimer.
http://www.ion.ucl.ac.uk/library/patient/coffin.htm
Searchalot Directory For Coffin Lowry Syndrome
Sponsored Links. Top Health Conditions and Diseases Genetic Disorders CoffinLowry Syndrome (6). Related Web Sites.
http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Coff

Extractions: Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Genetic Disorders : Coffin Lowry Syndrome Related Web Sites Coffin-Lowry Syndrome Foundation - Information about the organization as well as CLS. Includes FAQs, news, links, parent and foundation contact details.
Directory :: Look.com
coffin lowry syndrome (6) Sites. coffin lowry syndrome Information sheet compiledby the National Institute of Neurological Disorders and Stroke (NINDS).
http://www.look.com/searchroute/directorysearch.asp?p=521012
Mioti: Medical Condition
not available. NORD coffin lowry syndrome. Condition coffin lowry syndrome. Neuromuscular Coffin LowrySyndrome.
http://www.mioti.com/cat/condition/condition.asp?Cat=CoffinLowry
Medicalseek - Search Engine For The Healthcare Industry
Conditions and DiseasesGenetic Disorderscoffin lowry syndrome coffin lowry syndromeInformation sheet compiled by the National Institute of Neurological
http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders_Coffin_Lowr
ClinicalTrials.gov - Linking Patients To Medical Research Basic
Search Clinical Trials. Enter words or phrases, separated by commas Tipslowry was not found. Select an alternative below or change your query.
http://www.clinicaltrials.gov/search/term=Coffin Lowry Syndrome
Listings Of The World Health Conditions And Diseases Genetic
Listings World Health Conditions and Diseases Genetic Disorderscoffin lowry syndrome. Listings World, Over 2
http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/Coffin
Canadian Directory Of Genetic Support Groups
Syndrome, Williams Syndrome) Cobalamin Network (Cobalamin (B12) Deficiency) CoffinLowrySyndrome Foundation (coffin lowry syndrome) Congenital Adrenal
http://www.lhsc.on.ca/programs/medgenet/c_sup.htm
Coffin Lowry Syndrome Website Results :: Linkspider UK
coffin lowry syndrome Websites from the Linkspider UK. coffin lowry syndromeDirectory. Complete Results for coffin lowry syndrome Related Topics.
http://www.linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Coffin

Extractions: Directory Tree: Top Health Conditions and Diseases Genetic Disorders : Coffin Lowry Syndrome (6) Add URL Advertise Here! Personalize Amazon ... Coffin-Lowry Syndrome Foundation - Information about the organization as well as CLS. Includes FAQs, news, links, parent and foundation contact details. Coffin Lowry Syndrome - Information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). NORD - General information about coffin lowry syndrome, its alternative names and further resources. Missouri Southern State College - Coffin lowry syndrome, an in depth article by Terry Patterson along with some images. National Library of Medicine - Coffin-Lowry syndrome, the synonyms, a summary and major features. Reader Digest Health - General information about The Coffin-Lowry Syndrome Foundation.
Coffin-Lowry Syndrome
coffinlowry syndrome information and resources, genetic information, support groups coffin-lowry syndrome. coffin-lowry syndrome Foundation. c/o Mary Hoffman
http://www.kumc.edu/gec/support/coffin_l.html
Coffin-Lowry Syndrome Foundation Welcome Page
Welcome. Welcome to The coffinlowry syndrome Foundation Home Page. coffin-lowrysyndrome Foundation. Attn Mary C. Hoffman. 3045 255th Avenue SE.
http://clsfoundation.tripod.com/Welcome.htm

Extractions: Welcome to The Coffin-Lowry Syndrome Foundation Home Page. The purpose of this web site is to provide a clearinghouse for information on Coffin-Lowry Syndrome (CLS), and to provide families affected by Coffin-Lowry syndrome a general forum in which to exchange information, ideas and advice. CLSF provides family matching services, telephone support, an informational database and publishes a newsletter, CLSF News. The newsletter is available in hard-copy and on this web site. CLSF is a non-profit organization and is funded solely by donations and change I find under the couch cushions. Contact CLSF at 425-427-0939 M-F after 6pm PST or at CLSFoundation@yahoo.com. Coffin-Lowry Syndrome Foundation Attn: Mary C. Hoffman 3045 255th Avenue S.E. Sammamish, WA 98075 ".....we can reject everything else: religion, ideology, all received wisdom. But we cannot escape the necessity of love and compassion... This, then, is my true religion, my simple faith. In this sense, there is no need for temple or church, for mosque or synagogue, no need for complicated philosophy, doctrine or dogma. Our own heart, our own mind, is the temple. The doctrine is compassion. Love for others and respect for their rights and dignity, no matter who or what they are: ultimately these are all we need. So long as we practice these in our daily lives, then no matter if we are learned or unlearned, whether we believe in Buddha or God, or follow some other religion or none at all, as long as we have compassion for others and conduct ourselves with restraint out of a sense of responsibility, there is no doubt we will be happy." His Holiness the Dalai Lama
Specific Diagnoses (C - D)
Anorectal Malformation; Cockayne syndrome; coffinlowry syndrome;coffin Siris syndrome; Cognitive Disability; Communication Disorders;
http://www.familyvillage.wisc.edu/card_cd.htm
Coffin-Lowry Syndrome Foundation
coffinlowry syndrome Foundation, a parent support group for families affectedby coffin-lowry syndrome. Thank you! coffin-lowry syndrome Foundation.
http://clsf.freeyellow.com/
BIBLIOGRAPHIE
Novel mutations in Rsk2, the gene for coffin-lowry syndrome (CLS). Eur. J.Hum. Genet. coffin-lowry syndrome and schizophrenia a family report.
http://alsace.u-strasbg.fr/chimbio/diag/coffin/biblio/

Extractions: laboratoire du Professeur Jean-Louis MANDEL du Professeur Charles SCHWARTZ du " GREENWOOD GENETICS CENTER " GREENWOOD USA BIBLIOGRAPHIE ID. Publication Abstract Abidi F, Jacquot S, Lassiter C, Trivier E, Hanauer A, Schwartz CE. Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS). Eur. J. Hum. Genet. (1999) 7: 20-26. Biancalana V., Briard ML., David A., Gilgenkrantz S., Kaplan J., Mathieu M., Piussan Ch., Poncin J., Shinzel A., Oudet C., Hanauer A Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. Am. J. Hum Gen. (1992) 50:981-987. Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PSN, O'Riordan JLH, Partington MW, Heyberger S, Oudet C, Hanauer A. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene. Genomics (1994) 22:617-625. Bird H, Collins AL, Oley C, Lindsay S. Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22. Am J Med Genet (1995) 59:512-516 SEQ Bjorbaek C, Vik TA, Echwald SM, Yang PY, Vestergaard H, Wang JP, Webb GC, Richmond K, Hansen T, Erikson RL, Gabor Miklos GL, Cohen PTW, Pederson O. Cloning of a human insulin-stimulated protein kinase (ISPK-1) gene and analysis of coding regions and mRNA levels of the ISPK-1 and the protein phosphatase-1 genes in muscle from NIDDM patients. Diabetes (1995) 44; 90-97.
COFFIN-LOWRY SYNDROME
Features Listed For coffinlowry syndrome. McKusick 303600. Coarse facialfeatures; Deafness, sensorineural; Delayed bone age; Flat malar region;
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?328
Health Library - Coffin-Lowry Syndrome
coffinlowry syndrome. Self Help Clearinghouse. The coffin-lowrysyndrome Foundation. International network. Founded
http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29c
Mutation Analysis In Coffin-Lowry Syndrome Patients
researchproject. Mutation analysis in coffinlowry syndrome patients.Following linkage analysis, families with one or several probands
http://www.research-projects.unizh.ch/med/unit42200/area313/p773.htm

Extractions: research project Mutation analysis in Coffin-Lowry syndrome patients Following linkage analysis, families with one or several probands affected with Coffin-Lowry syndrome were subjected to mutation anlysis in the CLS gene. Several hitherto undescribed mutations and a family with germline mosaicism were detected. Collaboration: physicians in Switzerland Publications Merienne et al. J Med Genet 1998;63:1153-1159 Jacquot et al. Eur J Hum Genet 1998;6:578-582 Contacts Prof. A. Schinzel schinzel@medgen.unizh.ch Dr. A. Hanauer (Project Leader) Last Update Responsible Project Leader: Dr. A. Hanauer Professor or Research Area Leader: Prof. Dr. Albert Schinzel Institute or Clinic: Faculty: Use the Eurospider retrieval system to find similar projects Use the Eurospider retrieval system to search the research report For authorized person(s) only Comments to uni research page generation 06.03.2003
Prof. Dr. Albert Schinzel
Hanauer. Mutation analysis in coffinlowry syndrome patients. Mutationanalysis in coffin-lowry syndrome patients. Hergersberg. Mutation
http://www.research-projects.unizh.ch/med/unit42200/area313/

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