41. Trisomy X Syndroom - MEDgle - Uw Symptomen Zoek symptoms, diagnosis, and references. http//en.wikipedia.org/wiki/fragile_x_syndrome http//www.medicinenet.com/fragile_x_syndrome/glossary.htm http://www.medgle.nl/?issearch=true§ion=keyword&keyword=trisomy X syndroom&g

42. Fragile X Syndrome Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/GB/fragile_x_syndrome.html

Orphanet database access Fragile X syndrome Direct access to data Alias FRAXA syndrome FRAXE syndrome FRAXF syndrome Fragile X syndrome type 1 Fragile X syndrome type 2 Fragile X syndrome type 3 Fragile X tremor / ataxia syndrome (FXTAS) Summary Full text http://www.orpha.net/data/patho/Pro/en/FragileXSyndrome-FRenPro120.pdf Clinical signs Behaviour disorder/autism Fragile site on X q 28 High forehead High vaulted/narrow palate Long/large/bulbous nose Macrodontia Macroorchidism/macrotestes Mental retardation (moderate/severe) Narrow face Prognathism Speech defect Thin lips Mental retardation(mild) E.E.G.abnormality Hyperextensible joints Seizures ( any type) Squint/paresis of ocular muscles Update : 15/04/2007 Orphanet database access Orphanet database access Fragile X syndrome Direct access to data Alias FRAXA syndrome FRAXE syndrome FRAXF syndrome Fragile X syndrome type 1 Fragile X syndrome type 2 Fragile X syndrome type 3 Fragile X tremor / ataxia syndrome (FXTAS) Summary Full text http://www.orpha.net/data/patho/Pro/en/FragileXSyndrome-FRenPro120.pdf Clinical signs Behaviour disorder/autism Fragile site on X q 28 High forehead High vaulted/narrow palate Long/large/bulbous nose Macrodontia Macroorchidism/macrotestes Mental retardation (moderate/severe) Narrow face Prognathism Speech defect Thin lips Mental retardation(mild) E.E.G.abnormality

43. Fragile X Syndrome - Kosmix Topic Page www.medicinenet.com/fragile_x_syndrome/article.htm. 1 2 3 Next ». View 40 More ». Trusted Sources». MedlinePlus Fragile X Syndrome http://www.kosmix.com/Health/fragile_x_syndrome-s

kapp.ads.cat1=''; kapp.ads.cat2='Support%3ADownSyndrome'; kapp.ads.cat3='fragile_x_syndrome'; kapp.ads.cat4='1406762040'; kapp.ads.cat5=''; htmlFileParams["size"] = "728x90"; htmlFileParams["w"] = "728"; htmlFileParams["h"] = "90"; htmlFileParams["site"] = "site224.tmus"; htmlFileParams["zone"] = "TopBanner1"; var site = htmlFileParams["site"]; var zone = htmlFileParams["zone"]; var h = htmlFileParams["h"]; var w = htmlFileParams["w"]; var size = htmlFileParams["size"]; var q = kapp.search.param["qtitle0"]; q = q.replace(/ /g, "+"); kapp.ads.dc_tile = kapp.ads.dc_tile + 1; var line = 'q=' + q + ';tile=' + kapp.ads.dc_tile + ';cat1=' + kapp.ads.cat1 + ';cat2=' + kapp.ads.cat2 + ';cat3=' + kapp.ads.cat3 + ';cat4=' + kapp.ads.cat4 + ';cat5=' + kapp.ads.cat5; document.write(''); moduleShown['ads_topban']=1 Fragile X Syndrome Topic Home Basic Facts Advanced Reading Community ... Shopping moduleShown['tabs']=1 moduleShown['ads_top']=0 Doctor-Reviewed Article Fragile X Syndrome Guide Definition Symptoms ... Prevention Fragile X syndrome is a genetic condition involving changes in part of the X chromosome. It is the most common form of inherited mental retardation in males and a ... Read More moduleShown['adam_callout']=1 See Also: Autism Doctor-Reviewed Article Fragile X syndrome Wikipedia Article Rett syndrome Wikipedia Article Web Categories for Fragile X Syndrome . Choose one. Learn The Basics Web Results Basic Facts Articles Trusted Sources Exchange Ideas

44. HANAMOKU - ディレクトリ検索 : トップ Translate this page . Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome. See also. Health Conditions and Diseases Neurological http://dir.hanamoku.jp/dmoz/Health/Conditions_and_Diseases/Genetic_Disorders/Fra

Health See also: Health: Conditions and Diseases: Neurological Disorders: Chromosomal Health: Mental Health: Disorders: Child and Adolescent: Mental Retardation: Causes Carolina Fragile X Project - A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them. Conquer Fragile X, Inc. - Creating a virtual research center in Israel to find a cure. Fragile X Association of Australia - Information on this disease, medical aspects, education, references, contacts and what's new in Australia Fragile X Association of Southern California - Fragile X Syndrome is the leading inherited cause of developmental disabilities and mental impairment worldwide. It affects 1 in 2,000 males and 1 in 4,000 females. It is estimated that 1 in 259 females are carries of the premutation. Fragile X Research Foundation of Canada - Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join. Fragile X Syndrome - Diagnostic and Carrier Testing - A Policy Statement from the American College of Medical Genetics. FRAXA Research Foundation Home Page - Non-profit organization run by parents. Fighting to find a cure for Fragile X Syndrome and helping Fragile X Family's.

45. Fragile X Syndrome - AspiesForFreedom See also. Autism. Retrieved from http//aspiesforfreedom.org/wiki/index.php? title=fragile_x_syndrome . Views. Article; Discussion; Edit; History http://www.aspiesforfreedom.org/wiki/index.php?title=Fragile_X_Syndrome

46. Fragile X Syndrome, Fragile X Syndrome Fact Sheets for Health Professionals. Contact numbers are Victorian. http://www.office-for-children.vic.gov.au/early-years-services/library/publicati

Advanced Site Search About the Division Site Map Site Help Languages Early Childhood Programs Early Childhood Programs Children's Week Early Childhood Intervention (ECIS) Maternal and Child Health ... In Home Support for Aboriginal Families Library Seminars and Conferences Newsletters FAQs Forms ... Fragile X Syndrome Fragile X Syndrome Content: definition differential diagnosis prenatal diagnosis management ... Disability Online Definition Fragile X syndrome (FXS) is now the most common known inherited cause of developmental disabilities, but was not discovered until the late 1970s. By 1980 it was found that people showing certain mental and physical characteristics had a chromosomal abnormality caused by a partial break on an X chromosome, called a "fragile site". In 1991 the Fragile X gene was identified within this site. The diagnosis of FXS is important to implement effective management and interventional strategies. Detection of carriers allows families to make informed decisions following genetic counselling. Incidence The Fragile X Syndrome Differential Diagnoses Developmental delay of different aetiology, hearing loss, autism and autism-like behaviours.

47. Daily Herald Search. search the entire directory, search this category only. Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome http://www.heraldextra.com/index.php?option=com_dwodp&c=/Health/Conditions_and_D

48. Fragile X Syndrome Sep 10, 2007 Quick Links. Select, A to Z Campus Index, Alumni Association, Athletics Recreation, Bookstore, Campus Health Centre, Career Services http://fhs.mcmaster.ca/main/news/news_2007/fragile_x_syndrome.html

MUGSI Quick Links Select A to Z Campus Index Alumni Association Bookstore Campus Health Centre Career Services Clubs Employers Financial Aid Find People @ McMaster Giving to McMaster Housing International Students Libraries Media MUGSI Login Policies Security Services Student Accounts Work/Study Abroad Working@McMaster Search McMaster FHS FHS News McMaster Home McMaster A-Z Index Academics Undergraduate Studies/Programs ... Learning Commons Faculty of Health Sciences Home About FHS Welcome from the Dean Introduction Video ... FHS Site Index Larger Text Smaller Text Print Stem cell research produces a key discovery for Fragile X Syndrome Published: September 10, 2007 Laurie Doering , associate professor in the Department of Pathology and Molecular Medicine. An important finding has been made by McMaster researchers about Fragile X Syndrome (FXS), a sex-linked genetic disorder that affects approximately one in 4,000 males and one in 6,000 females. FXS is the most common genetic disorder associated with mental impairment. The affected gene (FMR1) leads to inactivation of the FMR1 gene product, known as the fragile X mental retardation protein (FMRP). Brain development in the absence of this protein leads to cognitive effects, learning and memory problems, attention deficit, hyperactivity and autistic behaviours. Many children go undiagnosed with Fragile X.

49. Fragile X Syndrome - Indopedia, The Indological Knowledgebase Retrieved from http//www.indopedia.org/fragile_x_syndrome.html . This page has been accessed 241 times. This page was last modified 2332, http://www.indopedia.org/Fragile_X_syndrome.html

Indopedia Main Page FORUM Help ... Log in The Indology CMS In other languages: Deutsch Categories Disability Genetic disorders ... Wikipedia Article Fragile X syndrome ज्ञानकोश: - The Indological Knowledgebase Fragile X Syndrome is the most common cause of mental retardation , affecting approximately 1 in 1500 males and 1 in 3000 females . It is a genetic disorder caused by a mutation of the FMR1 gene on the X chromosome . Typically the FMR1 gene contains between 6 and 53 repeats of the CGG codon . In people with the disorder, the FMR1 allele has over 230 repeats. Expansion to such a degree results in a methylation of that portion of the DNA , effectively silencing the expression of the FRM1 protein . The characteristic constriction of the X chromosome at the chromosomal locus Xq27.3 is caused by this methylation. MI XlinkRecessive.jpg X-linked recessive inheritance Because men have only one copy of the X chromosome, males with sufficient trinucleotide expansion are symptomatic, while females have two X chromosomes and thus double the chance of a working allele (unless parents are related). Aside from

50. Armenia Search - Armenian Search Engine And Website Directory The Entire Web, Armenian Sites. Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome. See also. Health Conditions and Diseases http://www.armeniasearch.com/odp.php?browse=/Health/Conditions_and_Diseases/Gene

51. PepeDirectory: The Pepped Internet Directory entire PepeDirectory, only in Genetic_Disorders/fragile_x_syndrome. Top Health Conditions and Diseases Genetic Disorders Fragile X Syndrome (12) http://dir.pepesearch.com/cgi-bin/apexec.cgi?etype=odp&passurl=/Health/Condition

52. Fragile X Syndrome - Better Health Channel. Fragile X syndrome is an inherited condition that can cause various degrees of intellectual disability. It affects males more than females. http://www.betterhealthchannel.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Fragile_X_

53. Bigsearch.ca Directory Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome . See also. Health Conditions and Diseases Neurological Disorders http://directory.bigsearch.ca/directory.php?browse=/Health/Conditions_and_Diseas

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55. Lepidoptera http//www.wrongdiagnosis.com/f/fragile_x_syndrome/signs.htm; ^ Dölen G, Osterweil E, Rao BS et al. (2007). Correction of fragile X syndrome in mice . http://www.mainstoreb.vot.pl/?title=Fragile_X_syndrome

56. InternetStart.dk - Danmarks Bedste Personlige Startside Med Flotte Baggrunde, Po the entire directory, only in Genetic_Disorders/fragile_x_syndrome. Index Health Conditions and Diseases Genetic Disorders Fragile X Syndrome (12) http://www.internetstart.dk/dmoz/?type=cat&path=/Health/Conditions_and_Diseases/

57. Fragile X Syndrome Fragile X Syndrome. Lab studies request form CPT Codes/Price List (PDF). Fragile X Syndrome is the most common form of inherited mental retardation. http://www.ggc.org/Diagnostics/Molecular/fragile_x_syndrome.htm

Fragile X Syndrome Contact Site Index Search GGC Website var MenuLinkedBy="AllWebMenus [4]",awmMenuName="mainmenubar",awmBN="638";awmAltUrl=""; Fragile X Syndrome Lab studies request form CPT Codes/Price List (PDF) Fragile X Syndrome is the most common form of inherited mental retardation. More than 99% of cases are due to the expansion of a polymorphic (CGG) repeat within the FMR1 gene. Approximately 1/1250 males and 1/2500 females are affected by the condition. Some population studies have shown the carrier frequency to be as high as 1/250 individuals. The American College of Medical Genetics policy statement on Fragile X testing recommends consideration of testing under the following circumstances: Individuals of either sex with mental retardation, developmental delay, or autism Individuals with a family history of Fragile X syndrome or unexplained MR Prenatal testing of fetuses of known carrier mothers Patients with negative cytogenetic fragile X testing results who have clinical symptoms of Fragile X syndrome Fragile X testing at the Greenwood Genetic Center involves two independent molecular approaches. Southern blotting and subsequent analysis allows the repeat segment size and methylation status of a sample to be determined. Polymerase chain reaction analysis is utilized to more accurately determine (CGG) repeat numbers in high normal and premutation ranges. Prenatal testing is available, please contact the

58. English Literature & Creative Writing Web Sites, Resources For Writers & Informa Search the web. search the entire directory, search this category only. Top Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome http://www.literature-study-online.com/search/index.php/Health/Conditions_and_Di

Literature > Authors > English Literature > American Literature > ... All Books > Search the web: search the entire directory search this category only Top Health See also: Health: Conditions and Diseases: Neurological Disorders: Chromosomal Health: Mental Health: Disorders: Child and Adolescent: Mental Retardation: Causes Carolina Fragile X Project - A series of studies examining the impact of fragile X syndrome (FXS) on individuals, families and the agencies that serve them. Conquer Fragile X, Inc. - Creating a virtual research center in Israel to find a cure. Fragile X Association of Australia - Information on this disease, medical aspects, education, references, contacts and what's new in Australia Fragile X Association of Southern California - Fragile X Syndrome is the leading inherited cause of developmental disabilities and mental impairment worldwide. It affects 1 in 2,000 males and 1 in 4,000 females. It is estimated that 1 in 259 females are carries of the premutation. Fragile X Research Foundation of Canada - Registered charity publishes a newsletter, invites applications for research grant, and explains how to donate or join. Fragile X Syndrome - Diagnostic and Carrier Testing - A Policy Statement from the American College of Medical Genetics.

59. Fragile X Syndrome In Mediseek Fragile X syndrome / From Wikipedia / Jump to navigation, search In people with the fragile X http//en.wikipedia.org/wiki/fragile_x_syndrome http://mediseek.seekport.co.uk/topic/fragile_x_syndrome/

Browse by alphabet A B C D ... Z Common search terms lens capsule postmature syncope levocarnitine ... allotypic marker Pages for fragile x syndrome Fragile X Syndrome - March of Dimes ... How is fragile X syndrome diagnosed? ... What causes fragile X syndrome ? ... How is... http://www.marchofdimes.com/professionals/14332_9266.asp Fragile X syndrome - Wikipedia Fragile X syndrome / From Wikipedia / Jump to: navigation, search ... In people with the fragile X http://en.wikipedia.org/wiki/Fragile_X_syndrome Fragile X Syndrome: Chromosomes Fragile X Syndrome affects males and females differently. ... The mutation in the FMR1 ( Fragile X Mental Retardation Protein)... http://www.lycos.com/info/fragile-x-syndromechromosomes.html Facts About Fragile X Syndrome ... In some cases, a single copy of the Fragile X gene is sufficient to cause the syndrome in females. ... " Eventually, the mutation reaches a critical number of repeats... http://www.childdevelopmentinfo.com/disorders/facts_about_fragile_x_syndrome.htm FRAGILE X SYNDROME Medic8® Family Health Guide ... What is Fragile X syndrome Fragile X syndrome is the most common form...

60. ODP - Open Directory Project It is constructed and maintained by a vast, global community of volunteer editors. Health Conditions_and_Diseases Genetic_Disorders fragile_x_syndrome http://www.venuecom.com/odp/Health/Conditions_and_Diseases/Genetic_Disorders/Fra

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