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Carrier testing for spinal muscular atrophy

Academic Article
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Overview

authors

  • Gitlin, J. M.
  • Fischbeck, K.
  • Crawford, T. O.
  • Cwik, V.
  • Fleischman, A.
  • Gonye, K.
  • Heine, D.
  • Hobby, K.
  • Kaufmann, P.
  • Keiles, S.
  • MacKenzie, A.
  • Musci, T.
  • Prior, T.
  • Lloyd-Puryear, M.
  • Sugarman, E. A.
  • Terry, S. F.
  • Urv, T.
  • Wang, C.
  • Watson, M.
  • Yaron, Y.
  • Frosst, Phyllis
  • Howell, R. R.

publication date

  • October 2010

journal

  • Genetics in Medicine  Journal

subject areas

  • Female
  • Genetic Carrier Screening
  • Genetic Counseling
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Heterozygote
  • Humans
  • Muscular Atrophy, Spinal
  • National Institutes of Health (U.S.)
  • Practice Guidelines as Topic
  • Pregnancy
  • Prenatal Diagnosis
  • Standard of Care
  • United States
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Research

keywords

  • carrier screening
  • meeting report
  • national standards
  • policy
  • spinal muscular atrophy
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Identity

International Standard Serial Number (ISSN)

  • 1098-3600

Digital Object Identifier (DOI)

  • 10.1097/GIM.0b013e3181ef6079

PubMed ID

  • 20808230
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Additional Document Info

start page

  • 621

end page

  • 622

volume

  • 12

issue

  • 10

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