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klinefelter.it - This website is for sale! - sindrome di klinefelter,disgenesia dei tubuli seminiferi Resources and Information. | klinefelter.it Reviews
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KLINEFELTER SYNDROM Österreich - Home
In Zusammenarbeit mit den. Netzwerk für Österreich und Deutschland. Unsere Veranstaltungen findet Ihr auf. Gemeinsam für Selten - Rare Disease Salzburg. Gedanken an Frau Dr. Brigitte Esterbauer. Klinefelter Syndrom Folder - weitere Unterlagen unter Einleitung (Infomaterial). Danke an alle die uns Unterstützen. Bei allen Mitgliedern, Sponsoren die uns immer HELFEN,. Das unsere Arbeiten, Projekte und Veranstaltungen,. Immer ein Erfolg sind. Ich bin wie Du!
Klinefelter.be
Wat is het syndroom van Klinefelter? Is hier iets aan te doen? Wat houdt deze behandeling in? Hoe kan men lid worden? Welkom op de site van het syndroom van klinefelter . Op deze site kunnen jullie informatie vinden in verband met het syndroom. Langs het forum kunnen jullie praten over klinefelteronderwerpen en is het mogelijk om contacten te leggen. Verder vindt je informatie in verband met de bijeenkomsten. Indien vragen aarzel niet om te contacteren.
Klinefelter | Home
Vermittelt Kontakte zu Betroffenen. Gewährleistet absolute Diskretion. Diagnose Klinefelter-Syndrom - wie weiter? Sie haben von Ihrem Arzt / Labor den Befund Klinefelter-Syndrom erhalten? Unser Verein bietet umfassende Informationen Betroffener (Syndrom-Träger, Eltern, Partner, etc.) und vermittelt Ratsuchenden Kontakte. Fragen mit medizinischem Hintergrund. Fragen an Betroffene via.
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Herzlich willkommen auf unserer Webseite! Wir (die Deutsche Klinefelter-Syndrom Vereinigung e.V. - DKSV e.V.) sind eine 1992 gegründete, ehrenamtlich aktive Selbsthilfe-Organisation auf Bundesebene mit ca. 600 Mitgliedern. Unser Ziel ist es, Menschen mit Klinefelter-Syndrom, mit Klinefelter-Syndrom Sonderform (48xxxy und 49xxxxy) sowie deren Angehörige zu unterstützen. Treten Sie mit uns in Kontakt, telefonisch, per E-Mail oder im Forum! Folgen für die Betroffenen. Wie sage ich es meinem Kind?
Klinefelter.dk | Klinefelter Foreningen i Danmark
Klinefelter Foreningen i Danmark har nu Cvr. nr. Klinefelter Foreningen i Danmark. Formålet med denne side er, at komme i kontakt med alle jer andre her i Danmark, som enten selv er født med Klinefelter eller er forældre / ægtefælle / partner / sundhedsfaglig person til en med Klinefelter Syndrom. Desuden kan den lukkede og hemmelige gruppe IKKE findes ved søgninger, kun via invitation. 47xxy Klinefelter foreningen i Danmark. Vi glæder os, til at hører fra jer alle. Klinefelter Foreningen i Danmark.
klinefelter.it - This website is for sale! - sindrome di klinefelter,disgenesia dei tubuli seminiferi Resources and Information.
The domain klinefelter.it. May be for sale by its owner! This webpage was generated by the domain owner using Sedo Domain Parking. Disclaimer: Sedo maintains no relationship with third party advertisers. Reference to any specific service or trade mark is not controlled by Sedo nor does it constitute or imply its association, endorsement or recommendation.
Johns Hopkins Klinefelter Clinic
Johns Hopkins Klinefelter Syndrome Center. 1830 Monument Street, Suite 328,. Baltimore, MD 21287. WHAT IS KLINEFELTER SYNDROME. From the 1889 opening of The Johns Hopkins Hospital. To the opening of the School of Medicine. Four years later, there emerged the concept of combining research, teaching and patient care. This model, the first of its kind, would lead to a national and international reputation for excellence and discovery. About the KS Clinic. The goals of the clinic are:. To develop treatment g...
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Home - Nederlandse Klinefelter Vereniging
110;kv@klinefelter.nl. SvK en andere aandoeningen. Je weet het pas. Ouders & kinderen. Partners & betrokkenen. Leidraad Syndroom van Klinefelter. Over de Nederlandse Klinefelter Vereniging. Doelstelling, visie, missie. Meer info & links. Voor een beter leven met het Klinefeltersyndroom. SvK en andere aandoeningen. Je weet het pas. Ouders & kinderen. Partners & betrokkenen. Leidraad Syndroom van Klinefelter. Over de Nederlandse Klinefelter Vereniging. Doelstelling, visie, missie. Meer info & links. Lees a...
Klinefelterforeningen i Norge
Hjelp og støtte. Om ikonet i høyre hjørne. Nyttige linker og Videoer. Trenger du noen å snakke med? Velkommen til medlemenes Facebooksiden. Ta kontakt med : sirenel70@gmail.com. For adgang til gruppen. Info om Skjerm oppleser. XXYer en genetisk tilstand som rammer 1 av ca. 600 gutter. Diagnosen stilles ved en genetisk test fra en blodprøve. Tilstanden blir sjelden diagnostisert fordi symptomene likner til forveksling dem som også finnes i befolkningen forøvrig. Du kan hente den gratis [her].
KO Home
Announcement - New Publication: "The KS Story, you are not alone". To see previous announcements. Buy your Klinefelter Syndrome pin.
