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    Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis

    Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis

    Posted by colleen, Oct 17, 2019
    Click HERE to view the article on PubMed.gov.
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    Ocular manifestations in Gorlin-Goltz syndrome

    Posted by colleen, Sep 18, 2019
    Click HERE to view the article on PubMed.gov.

    Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome

    Posted by colleen, Jul 28, 2019
    Click HERE to view the article on PubMed.gov.

    Helping Your Child Transition To Adulthood

    Posted by admin, Jul 25, 2019
    Transitions, no matter what the age and personal situation can be a challenge. Add Gorlin syndrome to this and there is ...

    Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study

    Posted by colleen, Jul 20, 2019
    Click HERE to view the article on PubMed.gov.

    Tractor Pull & a BCCNS Alliance Member Makes for a Winning Combination

    Posted by admin, Dec 18, 2018
    The fourth annual Fall Smoke Out Truck and Tractor Pull on September 29, 2018 in Cadiz, OH, was a major success for raising ...

    Further Optimism for the Future

    Posted by admin, Dec 18, 2018
    A message from Julie Breneiser, BCCNS Alliance President

    The Difference a Phone Call Makes

    Posted by admin, Dec 01, 2018
    It’s about 8 o’clock and my day is starting to wind down. I’m sitting on the couch, relaxing and getting ready to watch some ...

    Kevin Gullat

    Posted by admin, Mar 28, 2018
    Being the spouse of someone with BCCNS (or any other condition for that matter) can be a challenge. I do not mean to imply ...

    Annewil Stelloo

    Posted by admin, Mar 28, 2018
    My name is Annewil, I am 30 years old and live in The Netherlands. In 2010 at age 27 I learned that I had Basal Cell ...

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    Email: info@gorlinsyndrome.org

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    Phone: 267-689-6443

     

    Join the GSA Community to find support, empowerment and hope. You are not alone.
     
    Our mission: to thoughtfully support, comprehensively educate, and aggressively seek the best treatments and a cure for those affected by Gorlin syndrome.