41. Health Library - Robinow Syndrome Search. World class medicine. Hometown commitment. robinow syndrome. Self HelpClearinghouse. robinow syndrome Foundation. National network. http://www.phoebeputney.com/library/healthguide/SelfHelp/topic.asp?hwid=shc29rob

42. Health Library - Robinow Syndrome Services Affiliates. robinow syndrome. Self Help Clearinghouse. RobinowSyndrome Foundation. National network. Founded 1994 http://www.danhosp.org/library/healthguide/SelfHelp/topic.asp?hwid=shc29rob

43. Health Library - Robinow Syndrome Your Health, Advanced Search. robinow syndrome. Self Help Clearinghouse.robinow syndrome Foundation. National network. http://www.tetonhospital.org/library/healthguide/SelfHelp/topic.asp?hwid=shc29ro

44. Health Library - Robinow Syndrome Message From Our CEO Our Board of Trustees CCHM Foundation HealthSource, RobinowSyndrome. Self Help Clearinghouse. robinow syndrome Foundation. http://www.memorialhealthsource.com/library/healthguide/SelfHelp/topic.asp?hwid=

45. 166 The Gene For Autosomal Recessive Robinow Syndrome Is Located Program Nr 166 The gene for autosomal recessive robinow syndrome islocated in 9q. H. Van Bokhoven 1 , E. van Beusekom 1 , J. Celli http://www.faseb.org/genetics/ashg99/f166.htm

46. INVITED AND SPECIAL SESSIONS To be posted on poster board 2181/F. REPLACED BY Autosomal recessiverobinow syndrome is caused by homozygous mutations in ROR2 . http://www.faseb.org/genetics/ashg/ann-meet/2000-supp/2000-sess-34.htm

47. Directory :: Look.com robinow syndrome (4) See Also. Health Sites. NORD robinow syndrome Offersa general discussion, the synonyms and further resources. National http://www.look.com/searchroute/directorysearch.asp?p=552293

48. Directory :: Look.com Rheumatic Fever (7) Rheumatoid Arthritis (176) Rhinitis (28) RibGap Syndrome (4)Rickets (4) Riley-Day Syndrome (8) Ringworm (11) robinow syndrome (4) Rocky http://www.look.com/searchroute/directorysearch.asp?p=43360

49. Health Library - Robinow Syndrome Physician Search Nursery Net Ways of Giving. robinow syndrome. Self HelpClearinghouse. robinow syndrome Foundation. National network. http://www.altru.org/library/healthguide/SelfHelp/topic.asp?hwid=shc29rob

50. Links On Mental Retardation robinow syndrome. robinow syndrome, MCA/MR Syndromes, US NLM ROBINOWSYNDROME, OMIM robinow syndrome Foundation robinow syndrome, IBIS http://www.saunalahti.fi/kup/engl/links.htm

Finnish Information Center on Mental Retardation (in Finnish) English Links on Mental Retardation A B C D ... Z Aarskog Syndrome Pediatric Database OMIM Database ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, OMIM Acrodysostosis (Arkless-Graham syndrome) acrodysostosis, MCA/MR Syndromes, US NLM Acrodysostosis, UNIVERSITY OF MARYLAND MEDICINE ACRODYSOSTOSIS, OMIM Acrodysostosis, NORD ... Acrodysostosis, Orphanet Aphasia The Family Village Library, Aphasia Page What is Aphasia? AGU Syndrome, Aspartylglucosaminuria ASPARTYLGLUCOSAMINURIA; AGU (OMIM) aspartylglycosaminuria, U.S. National Library of Medicine Alagille Syndrome Alagille syndrome (AGS), U.S. National Library of Medicine ALAGILLE SYNDROME; AGS, OMIM The Official Alagille Syndrome Alliance Worldwide Web Site Alagille Syndrome, GeneClinics Web site Allan-Herndon Syndrome OMIM, MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA Alopecia-Mental Retardation (AMR) Syndrome ALOPECIA-MENTAL RETARDATION SYNDROME, OMIM alopecia-mental retardation (AMR) syndrome, MCA/MR Syndromes, US NLM Alopecia mental retardation syndrome, Orphanet Alternating hemiplegia of childhood Omim Database, Alternating hemiplegia of childhood

51. Robinow Syndrome robinow syndrome. SK Singh*, SK Bhadada*, R Singh**, SK Sinha*, SK Singh***,JK Agrawal****. Abstract. robinow syndrome is a rare congenital abnormality. http://www.japi.org/august2000/c-Robinow Syndrome.htm

Case Report Robinow Syndrome SK Singh*, SK Bhadada*, R Singh**, SK Sinha*, SK Singh***, JK Agrawal**** *Senior Resident, **Junior Resident, Department of Pediatrics; ***Reader; ****Professor, Department of Endocrinology and Metabolism, Institute of Medical Sciences, Banaras Hindu University, Varanasi - 221 005. Received : 2.2.1999; Revised : 7.9.1999; Accepted : 8.1.2000 Abstract Robinow syndrome is a rare congenital abnormality. It is characterized by mesomelic brachymelia, hemivertebrae, dysmorphic facies, genital hypoplasia, micropenis, clinodactyly, camptodactly, hypoplastic nails and moderate short stature. We are documenting the case on the account of its rarity and additional features. (JAPI 2000; 48 : 836-837)

52. Health Library - Robinow Syndrome My Personal Health Site Search Advanced Search. robinow syndrome. Self HelpClearinghouse. robinow syndrome Foundation. National network. http://www.covenanthealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29r

53. Online And Offline Support: R R. robinow syndrome. robinow syndrome Foundation People served Individualsand families dealing with robinow syndrome; Services provided http://www.widesmiles.org/support/r.html

R Robinow Syndrome Robinow Syndrome Foundation People served: Individuals and families dealing with Robinow Syndrome Services provided: Information and support Address: 15955 Uplander Street NW, Andover MN 55304-2501 Phone number: (612) 434-1152 Contact person: Karla Kruger Romberg Syndrome/Parry-Romberg Syndrome The Rombergs Connection and The Romberg's Connection Annex People served: Individuals dealing with Rombergs Syndrome Services provided: Information and support Email address: rombergs@hotmail.com Main Website: http://www.geocities.com/HotSprings/1018/ Annex Website: http://www.geocities.com/HotSprings/Spa/4818/ Rubinstein-Taybi Syndrome Please note: Children, teens, and adults with Rubinstein-Taybi Syndrome have specific facial features that do not require reconstructive surgery. Rubinstein-Taybi Parent Group (RTPG) People served: Parents of children with Rubinstein-Taybi Syndrome Services provided: Support, parent-matching, information, and newsletter Address: PO Box 146, Smith Center KS 66967 Phone number: (785) 697-2984 Contact people: Garry and Lorrie Baxter Email address: lbaxter@ruraltel.net

54. WebMD - nord Robin Anomalad nord Robin Sequence nord Robin Syndrome nord RobinowDwarfism nord robinow syndrome robinow syndrome nord robinow syndrome http://my.webmd.com/content/healthwise/34/8511.htm

WebMD Today Home WebMD Newscenter Member Services WebMD University My WebMD Find a Doctor, Clinic Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Family Genetics Who We Are About WebMD Health Mall Sponsored: Lose Lbs Naturally Heart Failure? Trouble Focusing? You are in Medical Library Choose a Topic Our Content Sources Health Guide A-Z Ask A Question Clinical Trials Health Topics Symptoms Medical Tests Wellness ... Support Organizations Search the Help All Topics Click a letter to see a list of topics beginning with that letter A B C D ... RU R r 18 [nord] back to top R( r(22) [nord] back to top R. R.I.D. (Remove Intoxicated Drivers) - Crime Victims / Offenders [shc] back to top r14 [nord] r15 [nord] ... back to top RA Rabies [mini-topic] Rabson-Mendenhall Syndrome [nord] Radial Aplasia-Amegakaryocytic Thrombocytopenia [nord] Radial Aplasia-Thrombocytopenia Syndrome [nord] ... back to top RC RCC [nord] back to top RD RDD [nord] back to top RE REACH ("Reassurance to Each") - Families of Mentally Ill [shc] Reaching Out - The WAGR Network - WAGR Syndrome [shc] Reachout of St. Lawrence County - Clearinghouse - New York [shc] Realtors Concerned for Realtors - Addictions [shc] ... back to top RF RF (Rheumatoid Factor) [medical-test-topic] back to top RG RGS [nord] back to top RH Rh Blood Typing [medical-test-topic] Rh Disease [major-topic] Rh Sensitization During Pregnancy [major-topic] Rheumatic Chorea [nord] ... Rheumatoid Arthritis, Juvenile [major-topic]

55. UK.SearchEngine.com - Finds It Fast! robinow syndrome. additional Robinow_Syndrome Categories robinow syndromeFoundation Details about the organization as well as the disease. http://uk.searchengine.com/Top/Health/Conditions_and_Diseases/Genetic_Disorders/

Home Top Health > Robinow Syndrome ADULT CARS SHOPPING FINANCE ... Robinow Syndrome Foundation - Details about the organization as well as the disease. Includes general information, a survey, newsletter and photos. National Library of Medicine - The synonyms of Robinow syndrome, a summary and a list of major features. NORD - Robinow Syndrome - Offers a general discussion, the synonyms and further resources. Yahoo! Groups - A new email group for sharing and learning about Robinow syndrome. Join, post and read from this site. WEBSEARCH POPULAR SEARCHES Auction Books Car Hire Cheap Flights ... Contact Us

56. Birth Disorder Information Directory - R Tetraphocomelia; SC Phocomelia Syndrome) List of Sites. robinow syndromeRecessive Form See Covesdem Syndrome. RobinowSorauf Syndrome http://www.bdid.com/defectr.htm

HOME R Rachischisis Rachischisis of the Spinal Cord Neural Tube defects - Pediatric Pathology (Includes a Photo) Iniencephaly with Rachischisis - Pediatric Pathology (Includes a Photo) Iniencephaly with Rachischisis and Encephalocele - Pediatric Pathology (Includes a Photo) Radiodigitofacial Dysplasia See Van Goethem Syndrome Radioreno-Ocular Syndrome See Acrorenoocular Syndrome Ramer Ladda Syndrome (Brachydactyly Deafness Skeletal Anomalies) brachydactyly deafness skeletal anomalies Ramon Syndrome (Cherubism Gingival Fibromatosis Mental Retardation) Cherubism gingival fibromatosis mental retardation RAMON SYNDROME Ramos Arroyo Clark Syndrome (Corneal Anesthesia Deafness Mental Retardation) Corneal anesthesia deafness mental retardation Corneal Hypesthesia with Retinal Abnormalities, Sensorineural Deafness, Unusual Facies, Persistent Ductus Arteriosus, and Mental Retardation Rapp Hodgkin Syndrome (Ectodermal Dysplasia, Anhidrotic, with Cleft Lip and Cleft Palate) ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP AND CLEFT PALATE Reardon Wilson Cavanagh Syndrome (Ataxia and Deafness, Reardon Type; A taxia- D eafness- R etardation [ ADR ] Syndrome) Ataxia deafness reardon type ATAXIA-DEAFNESS-RETARDATION SYNDROME Also see Red Hair Color Red Hair Color (Hair Color 2) HAIR COLOR 2; HCL2

57. Birth Disorder Information Directory - CO-CZ Covesdem Syndrome (Costovertebral Segmentation DefectMesomelia; robinow syndrome, Recessive Form) http://www.bdid.com/defectco.htm

HOME Co-Cy COACH Syndrome See Cerebellar Vermis Hypo/Aplasia, Oligophrenia, Congenital Ataxia, Ocular Coloboma, and Hepatic Fibrosis (COACH) Syndrome Coarctation of (the) Aorta (CoA) List of Sites Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Coats disease Cobb Syndrome Syndromes associated with AVMs Cocaine Antenatal Infection See Fetal Cocaine Syndrome Related Books Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Keratosis palmoplantaris periodontopathia KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS Cockayne Syndrome List of Sites COD-MD Syndrome See Walker Warburg Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Cerebro oculo dento auriculo skeletal syndrome CODAS SYNDROME Coffin Syndrome (Arthritis Short Stature Deafness) Coffin syndrome Coffin-Lowry Syndrome List of Sites Coffin Siris Syndrome (Fifth Digit Syndrome) Coffin siris syndrome FIFTH DIGIT SYNDROME COFS Syndrome See Cerebrooculofacioskeletal (COFS) Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen hayden syndrome Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) blepharophimosis ptosis syndactyly mental retardation Cohen Syndrome List of Sites Colavita Kozlowski Syndrome (Short Limb Dwarf, Lethal Colavita Kozlowski Type)

58. Poster 316 - Mutations In ROR2 Which Give Rise To Autosomal Recessive Robinow Sy HGM2001 Poster Abstracts 10. Disease Mechanisms. POSTER NO 316. Mutationsin ROR2 which give rise to autosomal recessive robinow syndrome. http://hgm2001.hgu.mrc.ac.uk/Abstracts/Publish/WorkshopsPoster/WorkshopPoster10/

HGM2001 Poster Abstracts: 10. Disease Mechanisms POSTER NO: 316 Mutations in ROR2 which give rise to autosomal recessive Robinow syndrome Ali R. Afzal Nagwa A. Meguid, Michael A. Patton, Steve Jeffery Medical Genetics Unit, St George’s Hospital Medical School, London Human Genetics Department, National Research Centre, Cairo, Egypt. The Autosomal Recessive form of Robinow syndrome (RRS) is a severe skeletal dysplasia with generalised limb bone shortening, segmental defects of the spine, brachydactyly and a dysmorphic facial appearance. Previously we mapped and identified the gene mutated in RRS, and this is ROR2, located on chromosome 9q22. ROR2 encodes an orphan receptor tyrosine kinase and mutations in this gene are also responsible for brachydactyly type B, which is an autosomal dominant condition. We studied different probands from consanguineous families and found homozygous missense mutations and also a nonsense mutation in this gene in these patients. In the present study we present new mutations identified in this gene and discuss the possible mechanism by which these mutations cause autosomal recessive Robinow syndrome. Other abstracts in same session

59. Listings Of The World Health Conditions And Diseases Genetic Listings World Health Conditions and Diseases Genetic Disordersrobinow syndrome. Listings World, Over 2 million http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/Robino

60. EnableNet - Enablenet.browse.browse Physical Disabilities MusculoSkeletal Disorders robinow syndrome robinow syndrome Matching Resources. Records 1-1 of 1 http://www.enable.net.au/index.cfm?fuseaction=enablenet.browse.browse&catid=2219

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