نتائج البحث 151-160 من 14489 لعملية البحث عن Single+nucleotide+polymorphisms

  1. طب الأعصاب - التجارب السريرية - Mayo Clinic (مايو كلينك)

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  2. التجارب السريرية - مركز مايو كلينك للأطفال

    ... one parent is known by prior genetic testing to have a mutation in one of the common LQTS genes: potassium voltage-gated channel subfamily Q member 1 (KCNQ1) ...

  3. طب الأعصاب - التجارب السريرية - Mayo Clinic (مايو كلينك)

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  4. publications - المتخصصون في المجالات الطبية - Mayo Clinic

    Mayo Clinic Proceedings. Journal. One of the nation's largest-circulation medical journals, published monthly. Visit site. Mayo Clinic Scientific Press. Guides ...

  5. طب الأعصاب - التجارب السريرية - Mayo Clinic (مايو كلينك)

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  6. NF2-related schwannomatosis (neurofibromatosis type 2) - الأعراض والأسباب - Mayo Clinic (مايو كلينك)

    These tumors can include meningiomas, other schwannomas or ependymomas in the spinal cord. NF2-related schwannomatosis is one type of schwannomatosis, a group ...

  7. طب الأعصاب - التجارب السريرية - Mayo Clinic (مايو كلينك)

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

  8. التجارب السريرية - مركز مايو كلينك للأطفال

    ... one parent is known by prior genetic testing to have a mutation in one of the common LQTS genes: potassium voltage-gated channel subfamily Q member 1 (KCNQ1) ...

  9. Brainstem tumor - الأعراض والأسباب - Mayo Clinic (مايو كلينك)

    Some tumors grow slowly in one area while others spread more widely through nearby tissue. A tumor may appear as a single mass or as multiple spots.

  10. متلازمة بويتز-جيغرز - الأعراض والأسباب - Mayo Clinic (مايو كلينك)

    Family history is the main risk factor for Peutz-Jeghers syndrome. A person needs only one changed copy of the STK11 gene to have the condition. So if either ...