Carrier testing for spinal muscular atrophy

Academic Article

• Overview
• Research
• Identity
• Additional Document Info
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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

Research

keywords

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

Identity

International Standard Serial Number (ISSN)

• 1098-3600

Digital Object Identifier (DOI)

• 10.1097/GIM.0b013e3181ef6079

PubMed ID

• 20808230

Additional Document Info

start page

• 621

end page

• 622

volume

• 12

issue

• 10