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

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 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
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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.
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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

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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)

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

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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/
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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