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         Rubinstein-taybi Syndrome:     more detail
  1. Dysostoses: Syndrome D'apert, Syndrome de Rubinstein-Taybi, Syndrome Oro-Facio-Digital Type 1, Syndrome de Greig, Syndrome de Pfeiffer (French Edition)
  2. Rubinstein-Taybi syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Java, MS Solis, 2005
  3. Rubinstein-Taybi Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  4. Cornelia de lange syndrome / maple syrup urine disease / Rubinstein-Taybi syndrome: behavior issues, activities, and conclusions.: An article from: Palaestra by Robert C. Weber, 2006-03-22
  5. Consanguineous Marriages in the American Population by George B. Louis Arner, 2010-08-10

81. Rubinstein Taybi Syndrome MTA
Materials Transfer Agreement (rubinsteintaybi cosmids). This Agreementis entered into by and between 1) Leiden University (hereinafter
http://www.lgtc.nl/main/services/general/rts_mta.htm
Materials Transfer Agreement (Rubinstein-Taybi cosmids)
This Agreement is entered into by and between: 1) Leiden University (hereinafter referred to as PROVIDER), more specifically the Department of Human Genetics of the Leiden University Medical Center, headed by Prof. Dr. G.J.B. van Ommen, with its principal place of business at: Wassenaarseweg 72, 2333 AL LEIDEN, the Netherlands and 2) ................................................... (name), recipient investigator, acting for and on behalf of
........................................................... (institute/address), hereinafter referred to as "the Institute" WHEREAS PROVIDER is the owner of the RT100, RT102, RT166, RT191 and RT203 cosmids , with the product description specified in Attachment I and of the associated information, know-how and patent applications (hereinafter collectively referred to as "PROBE"); WHEREAS PROVIDER is willing to make available to third parties PROBE and specific related information considered proprietary (hereinafter referred to as "the Confidential Information") to third parties, provided a Material Transfer Agreement in the format hereof (hereinafter referred to as "an MTA") has been executed by such third parties; WHEREAS the Institute wishes to obtain the PROBE for a non-commercial research project to be performed in its own laboratories;

82. Sindrome Rubinstein Taybi Syndrome Bambi

http://fastnet.it/enti/bambi/sindrome-rubinstein-taybi.htm
Sindrome Rubinstein Taybi Rubinstein Taybi Syndrome
http://www.bdp.it/disabili/forum/viewforum.php3?boardid=1

.it
http://www.familyvillage.wisc.edu/lib_rub.htm

http://www.rubinstein-taybi.org

http://www.cafamily.org.uk/Direct/r36.html

http://doctorbbs.com/ipes/arts.html
...
http://www.specialink.com/e-curbcuts/MainCategories/Assistance/rubinstein.ht
m
http://www.rubinstein-taybi.org/bluebook/behavioral_issues_in_rubinstei.html

http://georgia.ncl.ac.uk/URODwSMLS/IWS/Rs/RT.html

http://www.worldmedicus.com/servlet/Controller/$7006000b307f0000.sj_viewi/
http://medlineplus.adam.com/ency/article/001249.htm ... http://ask.oxygen.com/AnswerFinal.asp?Link=http://thriveonline.oxygen.com/me n=0 http://www.kumc.edu/gec/support/rubinste.html http://iwhome.com/rts/Articles/Pamplet/Portugese/portugese.htm http://cadernodigital.uol.com.br/guiadobebe/artigos/sindromerubinstein.htm http://www.crosswinds.net/~ospecialchildren/databank/sindrome/rts/rts_index .htm http://www.entreamigos.com.br/temas/defmenta/sinrubi.htm http://www.rubinstein-taybi.org/html/messages/17.html La sindrome di Rubinstein e Taybi è una malattia genetica rara multisistema che colpisce molti organi del corpo. L'insieme di fattori associati a

83. AFSRT / L'Olivier - Association Française Du Syndrome De
Translate this page L'Olivier Association Française du syndrome de rubinstein-taybi (AFSRT) 19 rueChauffour, 33000 BORDEAUX Tél. 05 56 98 85 69 .
http://perso.wanadoo.fr/afsrt-olivier/
Choisissez votre langue
L'Olivier
Association Française du Syndrome de
RUBINSTEIN-TAYBI (A.F.S.R.T.)
19 rue Chauffour, 33000 BORDEAUX
Tél. : 05 56 98 85 69
Depuis le 23 Avril 2001 vous êtes le ème visiteur Dernière mise à jour : le 12 Mars 2003 Affichage optimal en 800 x 600
DenisPerso

84. Rubinstein Taybi Syndrome Support Group, Cincinnati Childrens Hospital Medical C
Pediatric Rehabilitation. Polio. Rubinstein Taybi syndrome. Overview. How to ReachUs. Vision. Young Adults Coping With Arthritis. rubinstein taybi syndrome. Overview.
http://www.cincinnatichildrens.org/Your_Visit/Patient_Family_Activities/Support
Overview Special Needs Kids' Summer Camps Resources Support Groups ... Polio Rubinstein-Taybi Syndrome Sudden Infant Death Syndrome Turner Syndrome Velocardiofacial Verbal Apraxia ... Visual Impairment
Support Groups
Rubinstein-Taybi Syndrome
Children's Hospital Medical Center provides support for patients and families through the Family Resource Center and the Rubinstein-Taybi Syndrome Support Group. Contact Us
For more information, call 785-697-2984 or visit the Rubinstein-Taybi web site
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85. Associação Rubinstein-Taybi Síndrome
Translate this page O que é a Síndrome de rubinstein-taybi? Características. Caracterizama Síndrome de rubinstein-taybi os seguintes sinais e sintomas
http://doctorbbs.com/ipes/arts.html
Missão
A necessidade de levar informações sobre a síndrome Rubinstein-Taybi para a comunidade médica e familiares dos portadores do Brasil resultou na recente formação da Associação Brasileira dos Familiares e Amigos dos Portadores da síndrome de Rubinstein-Taybi no Brasil (ARTS). A associação, instalada no bairro da Vila Madalena, em São Paulo, começa suas atividades buscando detectar mais portadores da síndrome no Brasil e realizar um trabalho multidisciplinar de integração social do portador da síndrome.
O que é a Síndrome de Rubinstein-Taybi?
    Características
    Síndrome é um termo médico designado a qualquer combinação de sinais e sintomas que indiquem a existência de uma condição, um problema, etc.
    Caracterizam a Síndrome de Rubinstein-Taybi os seguintes sinais e sintomas:
  • Geralmente, o portador na fase de zero a dois anos engasga com líquido, bebendo pouco e de forma lenta, têm acessos de vômitos constantes, apresentam resfriados ou broncopneumonias recorrentes e apnéia de sono obstrutiva (roncam enquanto dormem).
  • O hálux (dedão do pé) e o polegar são largos e grandes.

86. Rubinstein Taybi Syndrome UK Support Group

http://www.rtsuk.org/
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87. Rubinstein Taybi Syndrome UK Support Group - Welcome Page
Welcome to the Rubinstein Taybi syndrome UK Support Group. The grouphas been offering support for a number of years to parents with
http://www.rtsuk.org/home.htm
Welcome to the Rubinstein Taybi Syndrome UK Support Group
The group has been offering support for a number of years to parents with children affected by Rubinstein Taybi Syndrome. Initially, support was given by one mum who kept in touch with everyone by telephone or letter. To make use of today's technologies, www.RTSUK.org was set-up to provide information on RTS to a wider audience.
Latest News
Autumn 2002 Newsletter
There is a new format for the Autumn 2002 RTS newsletter thanks to Maxine Aldred ( Click here to view
RTS Booklet
free of charge from any committee member.
more news...
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To navigate around this site simply click on any of the categories within the contents panel on the left side of this page. It is advisable to have your screen size set to a minimum of 800x600 and the browser maximised to full screen. This complexity of this website has been kept to a minimum to provide a user-friendly interface and to reduce the time needed to download pages. If you have any comments on, or would like to contribute to the website, please send an email to

88. NORD - National Organization For Rare Disorders, Inc.
Rubinstein Taybi syndrome. To purchase fulltext report ($7.50) Copyright 1987,1989, 1992, 1997, 1998, 2002 Synonyms of Rubinstein Taybi syndrome
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Rubinstein Ta

89. Rubinstein – Taybi Syndrome, Cardiovascular Manifestation
Medical Professionals only. Rubinstein – taybi syndrome, cardiovascularmanifestation,, Print this article, (Jack Herbert Rubinstein
http://www.amershamhealth.com/medcyclopaedia/Volume V 2/RUBINSTEIN TAYBI SYNDRO
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*For Medical Professionals only, registration required Rubinstein – taybi syndrome, cardiovascular manifestation, (Jack Herbert Rubinstein, 20th century, American paediatrician; Hooshang Taybi, 20th century, American radiologist) a group of congenital anomalies consisting of short stature, mental retardation, characteristic facies, microcephaly and broad thumbs. Cardiovascular anomalies occur in about 20% of patients consisting of endocardial cushion defect atrial septal defect tetralogy of Fallot patent ductus arteriosus and ventricular septal defect
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90. A.F.S.R.T / L'Olivier - Association Française Du Syndrome De Rubinstein-Taybi
Translate this page L'A.F.S.R.T.a été fondée en Novembre 2000,par des parents, pour répondre aux attentes des familles et des enfants atteints par le Sydrome de
http://perso.wanadoo.fr/afsrt-olivier/index-general.html

91. A R T S B R A S I L . O R G . B R
Translate this page
http://www.artsbrasil.org.br/

92. WebGuest - Open Directory : Health : Conditions And Diseases : Rare Disorders :
Top Health Conditions and Diseases Rare Disorders RubinsteinTaybiSyndrome (4). See also Health Conditions and Diseases Genetic
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the entire directory only in Rare_Disorders/Rubinstein-Taybi_Syndrome Top Health Conditions and Diseases Rare Disorders : Rubinstein-Taybi Syndrome

See also:
Sites:
  • The CaF Directory - A desrciption of rubinstein taybi syndrome, its inheritance pattern, psychological and behavoural characteristics and a support group for those living in the United Kingdom.
  • HealthWise Knowledgebase - An article about Rubinstein-Taybi syndrome, a general discussion, symptoms, causes, incidence, treatment and resources.
  • Pediatric Database - An in depth look at rubinstein-taybi syndrome beginning with a definition, on to epidemiology, pathogenesis, clinical features, investigations and management.
  • Rubinstein Taybi Syndrome Support Group (UK) - Information, forum, links, contacts, and guestbook.
  • Rubinstein-Taybi Syndrome - A site devoted to the families and people diagnosed with this syndrome.

93. Corps

http://orphanet.infobiogen.fr/data/patho/FR/fr-SRT.html
Syndrome de Rubinstein-Taybi
Nom de la maladie et ses synonymes

Syndrome de Rubinstein-Taybi
Incidence
Description clinique
Mode de prise en charge incluant les traitements
Etiologie

CBP CBP CBP
Allanson JE. Rubinstein-Taybi syndrome : The changing face. Am J Med Genet 1990 ; 6 (suupl) : 38-41. Breuning MH, Dauwerse JG, Fugazza G et al. Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. Am J Hum Genet 1993 ; 52 : 249-54. Harth W, Linse R. [Dermatological stigmata in Rubinstein-Taybi syndrome] Hautarzt. 2001; 52: 977-9. Hennekam RCM, Lommeu EPJ, Strengers JCM, Van Spijker HG, Jansen-Kokx TMG. Rubinstein-Taybi syndrome in a mother and son. Eur J Pediatr 1989 ; 148 : 439-41. Hennekam RCM, Van Den Boogaard MJ, Sibbles BJ, Van Spijker HG. Rubinstein-Taybi syndrome in the Netherlands. Am J Med Genet 1990 ; 6 (suppl) : 17-29. Hennekam RCM, Tilanus M, Hamel BCJ et al. Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome : Clinical aspects. Am J Hum Genet 1993 ; 52 : 255-62. Kanitakis J, Claudy A. Rubinstein-Taybi syndrome (synonyms: Broad thumbs and great toes, characteristic facies, and mental retardation - Broad thumb-hallux syndrome). Eur J Dermatol. 2002 Jan-Feb;12(1):107-9.

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