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Phenotypic Involvement in Females with the FMR1 Gene Mutation.

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Bibliographic Details
Title: Phenotypic Involvement in Females with the FMR1 Gene Mutation.
Language: English
Authors: Riddle, J. E., Cheema, A., Sobesky, W. E., Gardner, S. C., Taylor, A. K., Pennington, B. F., Hagerman, R. J.
Source: American Journal on Mental Retardation. May 1998 102(6):590-601.
Peer Reviewed: N
Page Count: 12
Publication Date: 1998
Document Type: Journal Articles
Reports - Research
Descriptors: DNA, Eye Contact, Females, Genetics, Individual Characteristics, Learning Disabilities, Mental Retardation, Physical Characteristics, Severity (of Disability), Symptoms (Individual Disorders)
ISSN: 0895-8017
Abstract: A study investigated phenotypic effects seen in 114 females with premutation and 41 females (ages 18-58) with full Fragile X mental retardation gene mutation. Those with the full mutation had a greater incidence of hand-flapping, eye contact problems, special education help for reading and math, and grade retention. (Author/CR)
Entry Date: 1999
Accession Number: EJ568593
Database: ERIC
FullText Text:
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PubType: Academic Journal
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  Data: Phenotypic Involvement in Females with the FMR1 Gene Mutation.
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  Data: English
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  Data: <searchLink fieldCode="AR" term="%22Riddle%2C+J%2E+E%2E%22">Riddle, J. E.</searchLink><br /><searchLink fieldCode="AR" term="%22Cheema%2C+A%2E%22">Cheema, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Sobesky%2C+W%2E+E%2E%22">Sobesky, W. E.</searchLink><br /><searchLink fieldCode="AR" term="%22Gardner%2C+S%2E+C%2E%22">Gardner, S. C.</searchLink><br /><searchLink fieldCode="AR" term="%22Taylor%2C+A%2E+K%2E%22">Taylor, A. K.</searchLink><br /><searchLink fieldCode="AR" term="%22Pennington%2C+B%2E+F%2E%22">Pennington, B. F.</searchLink><br /><searchLink fieldCode="AR" term="%22Hagerman%2C+R%2E+J%2E%22">Hagerman, R. J.</searchLink>
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  Data: <searchLink fieldCode="SO" term="%22American+Journal+on+Mental+Retardation%22"><i>American Journal on Mental Retardation</i></searchLink>. May 1998 102(6):590-601.
– Name: PeerReviewed
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  Data: N
– Name: Pages
  Label: Page Count
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  Data: 12
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  Label: Publication Date
  Group: Date
  Data: 1998
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  Data: Journal Articles<br />Reports - Research
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  Data: <searchLink fieldCode="DE" term="%22DNA%22">DNA</searchLink><br /><searchLink fieldCode="DE" term="%22Eye+Contact%22">Eye Contact</searchLink><br /><searchLink fieldCode="DE" term="%22Females%22">Females</searchLink><br /><searchLink fieldCode="DE" term="%22Genetics%22">Genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Individual+Characteristics%22">Individual Characteristics</searchLink><br /><searchLink fieldCode="DE" term="%22Learning+Disabilities%22">Learning Disabilities</searchLink><br /><searchLink fieldCode="DE" term="%22Mental+Retardation%22">Mental Retardation</searchLink><br /><searchLink fieldCode="DE" term="%22Physical+Characteristics%22">Physical Characteristics</searchLink><br /><searchLink fieldCode="DE" term="%22Severity+%28of+Disability%29%22">Severity (of Disability)</searchLink><br /><searchLink fieldCode="DE" term="%22Symptoms+%28Individual+Disorders%29%22">Symptoms (Individual Disorders)</searchLink>
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  Data: 0895-8017
– Name: Abstract
  Label: Abstract
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  Data: A study investigated phenotypic effects seen in 114 females with premutation and 41 females (ages 18-58) with full Fragile X mental retardation gene mutation. Those with the full mutation had a greater incidence of hand-flapping, eye contact problems, special education help for reading and math, and grade retention. (Author/CR)
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  Data: 1999
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  Label: Accession Number
  Group: ID
  Data: EJ568593
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      – Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 12
        StartPage: 590
    Subjects:
      – SubjectFull: DNA
        Type: general
      – SubjectFull: Eye Contact
        Type: general
      – SubjectFull: Females
        Type: general
      – SubjectFull: Genetics
        Type: general
      – SubjectFull: Individual Characteristics
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      – SubjectFull: Learning Disabilities
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      – SubjectFull: Mental Retardation
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      – SubjectFull: Physical Characteristics
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      – SubjectFull: Severity (of Disability)
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      – SubjectFull: Symptoms (Individual Disorders)
        Type: general
    Titles:
      – TitleFull: Phenotypic Involvement in Females with the FMR1 Gene Mutation.
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            NameFull: Riddle, J. E.
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            NameFull: Cheema, A.
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            NameFull: Sobesky, W. E.
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            NameFull: Gardner, S. C.
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            NameFull: Taylor, A. K.
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              Y: 1998
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              Value: 102
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            – TitleFull: American Journal on Mental Retardation
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