Joies et difficultés du quotidien de Camille et d'autres enfants en France et à travers le monde, tous porteurs d'une anomalie chromosomique rare : une délétion 22q13, ou syndrome Phelan-McDermid. Site de l'association française du Syndrome Phelan-mcDermid.
http://www.22q13.fr/
TODAY'S RATING
>1,000,000
Date Range
HIGHEST TRAFFIC ON
Friday
LOAD TIME
3.5 seconds
16x16
32x32
PAGES IN
THIS WEBSITE
0
SSL
EXTERNAL LINKS
0
SITE IP
0.0.0.0
LOAD TIME
3.524 sec
SCORE
6.2
le site de Camille et de l'association française du Syndrome Phelan-McDermid | 22q13.fr Reviews
https://22q13.fr
Joies et difficultés du quotidien de Camille et d'autres enfants en France et à travers le monde, tous porteurs d'une anomalie chromosomique rare : une délétion 22q13, ou syndrome Phelan-McDermid. Site de l'association française du Syndrome Phelan-mcDermid.
My Site
This is my site description. Powered by InstantPage® from GoDaddy.com. Want one?
Default Parallels Plesk Panel Page
Web Server's Default Page. This page is generated by Parallels Plesk Panel. The leading hosting automation software. You see this page because there is no Web site at this address. You can do the following:. Parallels is a worldwide leader in virtualization and automation software that optimizes computing for consumers, businesses, and Cloud services providers across all major hardware, operating systems, and virtualization platforms. To find out more information. Hypervisor Virtualization technology for.
22q11 Hearts of Hope Foundation |
Welcome to 22Q11 Hearts of Hope. Perhaps you have found our website because. You or someone in your family has been diagnosed. With 22q11 deletion syndrome. If you are a teacher,. Physician, or a parent of a child with 22q11, please. Read through our information. We hope you will find. What is 22q11 DELETION SYNDROME? Because the signs and symptoms of 22q11 deletion syndrome are so varied, other names such as: DiGeore Syndrome, VCFS (velo cardio facial syndrome) and Shprintzen Syndrome are used to descri...
22q11 Ireland
Home Page
Velo-cardio-facial syndrome, also called 22q11.2 deletion syndrome, is caused by a small missing piece of genetic material from one copy of chromosome 22. Having even a small part of missing material may increase the risk of congenital anomalies, developmental delay and learning difficulties. The problems vary from person to person. We are a group of parents and professionals caring for children and adults with Chromosome 22q11.2 Deletion Syndrome.
le site de Camille et de l'association française du Syndrome Phelan-McDermid
Herzlich willkommen... | Deutsche Plattform für das Phelan-McDermid Syndrom
Deutsche Plattform für das Phelan-McDermid Syndrom. Was ist das Phelan-McDermid-Syndrom? The Phelan-McDermid Syndrom Foundation (PMS/PMD). Auf der Homepage des Vereins Phelan-McDermid-Gesellschaft e.V! Frisch gegründet wagen wir den Schritt von der Selbsthilfegruppe zum Verein!
Félicitations ! Votre domaine a bien été créé chez OVH !
Votre domaine 22q13.net. A bien été créé chez OVH. Accédez à votre Webmail OVH. Depuis votre Espace Client Web. Consultez la liste des. Vous pouvez dès à présent lui associer un hébergement,. En choisissant la solution la plus adaptée à vos besoins :. Pour héberger vos projets Web :. Site Internet, boutique en ligne,. Alliez la flexibilité du Cloud. À la liberté du dédié. Avec nos solutions VPS clef en main. Accompagnez vos projets Web. Vers une nouvelle étape. Hébergez vos sites Web.
PMSF - The Phelan-McDermid Syndrome Foundation Welcomes You To Our Official Site
What is Phelan-McDermid Syndrome? For PMSF Office use only. Click on the image above for more info) . . Click on the image above for more info). An International Alliance of Support and Science". PMSF International Family, Research Conference. July 20-23, 2016, in Orlando, Fla. Download our free PMSF conference phone app through the App Store. Traveling this summer with a child who has PMS? Planning can relieve some of the stress. Special toys and blankets must be packed to make our children feel at home...
Asociación Síndrome Phelan-McDermid
El Síndrome de Phelan-McDermid, o deleción del cromosoma 22q13, es una condición genética considerada enfermedad rara. Está causada en la mayoría de casos por la pérdida de material genético del extremo terminal del cromosoma 22. Esta pérdida se produce durante la división celular, cuando los cromosomas se alinean y replican, algunos de ellos se rompen y se pierden. Discapacidad intelectual de diversos grados. Ausencia o retraso del habla. Síntomas de autismo o Trastorno del Espectro Autista. Dolicocefal...
Home
Aconcagua Climb for 22q13 Deletion Foundation. Mar 6, 2010 - Aconcagua Climb Final Update. The 22q13 Deletion Foundation appreciates you. Feb 20, 2010 - Aconcagua Climb Update. Dan Fisk reached an altitude of 16,300 feet and is now returning to Mendoza. Extremely high winds turned back the majority of the 17 climbers that were apart of our group. Feb 18, 2010 - Aconcagua Climb Update. Dan Fisk is still climbing and going strong. Here's a link to Cern's photos ( Aconcagua Photos. Support the climb and rai...
