Top 100 alternative sites to smsresearchfoundation.org

  1. smith-magenis.org
    smith-magenis.org
  2. Supporting Families who have Children and Adults with Smith-Magenis Syndrome - Smith-Magenis Syndrome Foundation UK
    Help us support a fulfilling future for everyone living with Smith-Magenis syndrome We want to bring more families together, provide education and awareness training, and sponsor research into SMS. But we can’t do it without your help. We are the Smith-Magenis Syndrome (SMS) Foundation UK, and we support families who have children and adults with …

  3. smithmagenis.se
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  4. Föreningen Smith-Magenis syndrom

  5. smsaustralia.org
    smsaustralia.org
  6. Smith-Magenis Syndrome Australia |
    Has your child or loved one recently been diagnosed with Smith-Magenis Syndrome (SMS)? Are you seeking local connection and support? SMS Australia is a local not-for-profit organisation which drives awareness, support and a sense of community; enhancing the lives of children with SMS, and their families.

  7. prisms.org
    prisms.org
  8. PRISMS - Parents & Researchers Interested in Smith-Magenis Syndrome
    PRISMS is dedicated to providing information and support to families of persons with SMS

  9. smith-magenis.at
    smith-magenis.at
  10. Willkommen auf smith-magenis.at, der Webseite des Vereins Smith-Magenis-Syndrom Österreich - Smith-Magenis-Syndrom Österreich
    Willkommen auf den Seiten des Vereins Smith-Magenis-Syndrom Österreich. Wir bieten eine Anlaufstelle für Betroffene und Interessierte bzw Fachpersonal rund um das Smith-Magenis-Syndrom in Österreich.
    Author: Alexander Ströher

  11. smith-magenis.no
    smith-magenis.no
  12. Norsk forening for Smith-Magenis syndrom
    Norsk forening for Smith-Magenis syndrom arbeider for å spre informasjon og kunnskap om SMS syndrom til alle som ønsker det.

  13. smith-magenis.ch
    smith-magenis.ch
  14. Startseite - Smith-Magenis-Syndrom CH

  15. smithmagenis.es
    smithmagenis.es
  16. El síndrome de Smith Magenis – Síndrome Smith Magenis. Ayuda a familias.
    ¿Qué es el síndrome de Smith Magenis? No te pierdas ninguna de las publicaciones sobre

  17. smith-magenis.de
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  18. Sirius e.V. – Verein für Selbsthilfe, Information und Rat im Umgang mit dem Smith-Magenis-Syndrom

  19. smithmagenis.nl
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  20. Stichting Smith Magenis syndroom Nederland
    Stichting Smith Magenis syndroom Nederland is een samenwerkingsverband van ouders, familieleden, verzorgers en zorgprofessionals die zorgen voor of werken met kinderen of volwassenen met SMs

  21. smsbelgie.be
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  22. Smith Magenis Syndroom Belgie | SMsBE

  23. dsrf-uk.org
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  24. Down Syndrome Research Foundation | DSRF UK
    The DSRF UK Is A National Charity Formed By Parents Of Down’s Syndrome Children Who Want Greater Emphasis Placed On Medical Research.
    Author: Down's Syndrome Research Foundation

  25. thecutesyndrome.com
    thecutesyndrome.com
  26. The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research - Home - The Cute Syndrome Foundation
    Learn more about The Cute Syndrome Foundation and the SCN8A Epilepsy and PCDH19 Epilepsy Research we fund

  27. smithmagenis.is
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  28. Félag áhugafólks um Smith-Magenis heilkenni (SMS)
    Talið er að 1 af hverjum 25.000 séu með sjúkdóminn en hann orsakast af litningagalla og hefur mörg alvarleg og víðtæk einkenni. Við tökum vel á móti öllum nýjum einstaklingum sem vilja taka þátt og starfa fyrir félagið. Félagið tekur með þökkum á móti öllum styrkjum stórum sem smáum.
    Author: Admin

  29. globaldownsyndrome.org
    globaldownsyndrome.org
  30. Global Down Syndrome Foundation | Research, Care, Education, Advocacy  
    The Global Down Syndrome Foundation is dedicated to improving the lives of people with Down syndrome through research, medical care, education and advocacy.

  31. angelmanbehaviors.org
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  32. Angelman Syndrome Foundation | Welcome
    Angelman Syndrome Foundation
    Author: Angelman Syndrome Foundation

  33. irlensyndrome.org
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  34. Irlen Syndrome Foundation
    Visit the post for more.

  35. teamnoonan.org
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  36. Noonan Syndrome Foundation
    The Noonan Syndrome Foundation: created to help support, educate, & advocate for and on behalf of all those who have bee affected by Noonan Syndrome.

  37. fraxa.org
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  38. Fragile X Syndrome Research & Treatment • FRAXA Research Foundation - Finding a Cure for Fragile X
    FRAXA Research Foundation’s mission is to find effective treatments and ultimately a cure for Fragile X syndrome. Fragile X syndrome is the most common inherited cause of autism and intellectual disabilities We directly fund research grants and fellowships at top universities around the world. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments.
    Author: Holly Roos

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  39. lejeunefoundation.org
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  40. Jerome Lejeune Foundation USA - Down Syndrome Research, Care, and Advocacy
    The Jerome Lejeune Foundation USA centers its activities on Research, Care, and Advocacy for people with Down Syndrome.
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  41. csrf.net
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  42. CSRF - Cushing's Support & Research Foundation - Cushing's Syndrome Resources
    Cushing's Syndrome Resources

  43. loeysdietzcanada.org
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  44. Welcome to Loeys-Dietz Syndrome Foundation Canada | Loeys-Dietz Syndrome Foundation Canada

  45. dravetfoundation.org
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  46. Home - Dravet Syndrome Foundation
    Your Content Goes Here More News Dravet Syndrome Foundation is a non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form
    Author: Admin

  47. shwachman-diamond.org
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  48. Shwachman-Diamond Syndrome Foundation
    What is SDS? Shwachman Diamond Syndrome (SDS) is a rare blood disorder that affects the pancreas, bone marrow, and skeleton, but other organs may also be affected.

  49. loeysdietz.org
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  50. Loeys-Dietz Syndrome Foundation
    Our purpose is to provide information about what Loeys-Dietz Syndrome is and give hope to those impacted by the condition. We hope that you will find medical information and personal support to assist you and your family on your journey with Loeys-Dietz Syndrome. Learn more about our foundation and

  51. fmsfonline.org
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  52. False Memory Syndrome Foundation
    The False Memory Syndrome Foundation is a 501(c)(3) organization founded in March, 1992 to seek the reasons for the spread of the false memory syndrome, to work for ways to prevent the spread of the false memory syndrome, and to aid those who were affected by the false memory syndrome and bring their families into reconciliation.

  53. sjsupport.org
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  54. Welcome « Stevens Johnson Syndrome Foundation
    Stevens Johnson Syndrome Foundation

  55. barthsyndrome.org
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  56. Barth Syndrome Foundation : Home

  57. kdsf.org.my
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  58. Kiwanis Down Syndrome Foundation

  59. rettsyndrome.in
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  60. Indian RETT Syndrome Foundation

  61. cureangelman.org.au
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  62. Foundation For Angelman Syndrome Therapeutics

  63. christinacapozzifoundation.com
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  64. Funding Research for Shone's Syndrome
    The Christina Capozzi Foundation is a non-profit foundation which was formed to raise funds for research on heart disease at Childrens Hospital in Boston, MA.

  65. t21rs.org
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  66. T21RS – Down syndrome research

  67. pfdresearch.org
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  68. PFD Research Foundation | The Official Research Foundation of AUGS | PFD Research Foundation
    The PFD Research Foundation, formerly known as the AUGS Foundation, serves the medical profession by supporting promising, innovative research regarding the causes, prevention, cure and treatment of pelvic floor disorders.

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  69. bedfordresearch.org
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  70. Bedford Research Foundation - Bedford Research Foundation
    COVID-19 Testing at BRF The Bedford Research Foundation has expanded its regular non-profit laboratory services to offer fast and highly-accurate...

  71. researchfoundationofindia.com
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  72. Welcome to Research Foundation of India - Research Foundation of India
    Author: Admin

  73. omegaresearchfoundation.org
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  74. Welcome to Omega Research Foundation | Omega Research Foundation

  75. parkinsonhope.org
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  76. Parkinson Research Foundation | Parkinson Research Foundation

  77. tengocoin.org
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  78. Tengo Research Foundation
    World's first planetary Payment graph-based Blockchain Ecosystem.

  79. reyessyndrome.org
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  80. Reye's Syndrome | National Reye's Syndrome Foundation | United States
    In 1974, the National Reye's Syndrome Foundation, a children's health advocacy organization, was incorporated as a 501(c)3 charity, with a mission to eradicate the incidence of Reye's Syndrome. The Foundation does not receive, nor seek, government funding, and relies on the generosity of donors for support of all progr

  81. gouldsyndromefoundation.org
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  82. Gould Syndrome - COL4A1 - COL4A2 genes - Gould Syndrome Foundation
    Gould Syndrome Foundation a 501(c)3 Nonprofit, exists to provide hope and help to children and adults with the Ultra Rare Disease, Gould Syndrome; affecting COL4A1 and COL4A2 genes.
    Author: Jselser

  83. josephsmithfoundation.org
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  84. Joseph Smith Foundation | Remaining True to the Restoration - Joseph Smith Foundation

  85. sealy-smith-foundation.org
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  86. HOME | Sealy & Smith FoundationSealy & Smith Foundation
    Just another WordPress site
    Author: Admin

  87. udsf.org
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  88. Utah Down Syndrome Foundation : Home
    Author: John M Simmons

  89. mddsfoundation.org
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  90. Mal de Débarquement, Debarkation Syndrome | MdDS Foundation
    Mal de Débarquement, Disembarkment or Debarkation Syndrome is a disorder that leaves patients with a constant feeling of movement, as if on a boat. The MdDS Foundation advocates for and seeks treatments to end the suffering from MdDS. Learn more!
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  91. cureangelman.es
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  92. | FAST (Foundation for Angelman Syndrome Therapeutics)
    FAST España es una fundación, sin ánimo de lucro, creada por familias españolas con hijos afectados por el Síndrome de Angelman, con la finalidad de concienciar a la comunidad española y trabajar juntos por promover el desarrollo de terapias que propicien la cura y llevar el tratamiento a la práctica médica, actual, lo más rápido posible.

  93. fragilex.org
    fragilex.org
  94. The National Fragile X Foundation | Fragile X Syndrome
    The NFXF serves all those living with Fragile X, including awareness, research, and community for individuals and families at all stages of life.

  95. pmsf.org
    pmsf.org
  96. Home - Phelan-McDermid Syndrome Foundation
    Improving lives affected by Phelan-McDermid Syndrome Join Donate Newly Diagnosed International DataHub Upcoming Events Resource Library It is the mission of the Phelan-McDermid Syndrome Foundation to improve the quality of life of those affected by Phelan-McDermid syndrome worldwide by providing family support, accelerating research, and raising awareness. Latest News & Blog Post We are Phamily […]

  97. moebiussyndrome.co.za
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  98. Welcome to M S F A | Moebius Syndrome Foundation Africa (MSFA)

  99. rettsyndrome.org
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  100. Homepage | International Rett Syndrome Foundation
    Author: Kassie Morell; Mom; Kaylie age 4

  101. proteus-syndrome.org
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  102. Proteus Syndrome Foundation - Support and Education
    The Proteus Syndrome Foundation's goals are Supporting / Educating Families of individuals living with Proteus Syndrome, public education, research funding

  103. pks.org.au
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  104. Pallister-Killian Syndrome Foundation of Australia
    Pallister-Killian Syndrome Foundation of Australia
    Author: Catch Themes

  105. barthsyndrome.ca
    barthsyndrome.ca
  106. Barth Syndrome Foundation of Canada - Home

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  108. Restless Legs Syndrome Foundation Blog
    Support for those affected by restless legs syndrome (RLS). For more info visit www.rls.org.
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  109. rettresearch.org.au
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  110. Rett Research Australia – Rett Syndrome

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  112. Foundation for PIHMA Research & Education Foundation for PIHMA Research and Education - Foundation for PIHMA Research & Education

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  114. Home - Moebius Syndrome FoundationMoebius Syndrome Foundation | Home for the Moebius Community

  115. alsmithfoundation.org
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  116. The Alfred E. Smith Memorial Foundation
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  117. smith-barbieri.com
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  118. Smith-Barbieri | A Charitable Foundation

  119. kesmithfoundation.org
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  120. The Kelvin and Eleanor Smith Foundation
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  123. reverserett.org
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  124. Rett Syndrome Research Trust: The Trusted Source for Rett Syndrome Information
    Rett Syndrome Research Trust advances medical research, news and information about Rett Syndrome. A singular guide for parents and the scientific and medical community.

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  144. Umbanda Em Foco – Seu ponto de informação sobre politicas para o povo de santo.
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