Home  - Health_Conditions - Robinow Syndrome

Books Baby Camera Phones Computers Games DVD Electronics Kitchen Magazines Music Garden Software Tools Toys Video Apparel & Accessories Jewelry & Watches Musical Instruments Health & Personal Care Beauty Sports & Outdoors Office Products

e99.com Bookstore

Images

Newsgroups

41-60 of 90    Back | 1  | 2  | 3  | 4  | 5  | Next 20

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Robinow Syndrome:     more detail

Robinow syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS Polzin, 2005 Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02 Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-08-02 Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02 Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-06-20 Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-09-20 Anomalies And Curiosities Of Medicine- George M. Gould, A.M., M.D. by A.M., M.D. George M. Gould, 2010-02-17

lists with details

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

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
    
    Extractions: 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
    
    Extractions: R Robinow Syndrome Robinow Syndrome Foundation Romberg Syndrome/Parry-Romberg Syndrome The Rombergs Connection and The Romberg's Connection Annex 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

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/

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
    
    Extractions: HOME Rachischisis Radiodigitofacial Dysplasia Radioreno-Ocular Syndrome Ramer Ladda Syndrome (Brachydactyly Deafness Skeletal Anomalies) Ramon Syndrome (Cherubism Gingival Fibromatosis Mental Retardation) Ramos Arroyo Clark Syndrome (Corneal Anesthesia Deafness Mental Retardation) Rapp Hodgkin Syndrome (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) 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
    
    Extractions: HOME COACH Syndrome Coarctation of (the) Aorta (CoA) Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Cobb Syndrome Cocaine Antenatal Infection Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Cockayne Syndrome COD-MD Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Coffin Syndrome (Arthritis Short Stature Deafness) Coffin-Lowry Syndrome Coffin Siris Syndrome (Fifth Digit Syndrome) COFS Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) Cohen Syndrome 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/
    
    Extractions: 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.

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

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

41-60 of 90    Back | 1  | 2  | 3  | 4  | 5  | Next 20