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An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.

Publication ,  Journal Article
Tarleton, J; Richie, R; Schwartz, C; Rao, K; Aylsworth, AS; Lachiewicz, A
Published in: Hum Mol Genet
November 1993
Published version (DOI) Link to item

Duke Scholars

Ave Maria Lachiewicz
Author Ave Maria Lachiewicz Pediatrics, Neurology

Published In

Hum Mol Genet

DOI

10.1093/hmg/2.11.1973

ISSN

0964-6906

Publication Date

November 1993

Volume

2

Issue

11

Start / End Page

1973 / 1974

Location

England

Related Subject Headings

  • Sequence Deletion
  • Repetitive Sequences, Nucleic Acid
  • RNA, Messenger
  • Phenotype
  • Male
  • Intellectual Disability
  • Infant
  • Humans
  • Genetics & Heredity
  • Fragile X Syndrome
 

Citation

APA
Chicago
ICMJE
MLA
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Tarleton, J., Richie, R., Schwartz, C., Rao, K., Aylsworth, A. S., & Lachiewicz, A. (1993). An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype. Hum Mol Genet, 2(11), 1973–1974. https://doi.org/10.1093/hmg/2.11.1973
Tarleton, J., R. Richie, C. Schwartz, K. Rao, A. S. Aylsworth, and A. Lachiewicz. “An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.” Hum Mol Genet 2, no. 11 (November 1993): 1973–74. https://doi.org/10.1093/hmg/2.11.1973.
Tarleton J, Richie R, Schwartz C, Rao K, Aylsworth AS, Lachiewicz A. An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype. Hum Mol Genet. 1993 Nov;2(11):1973–4.
Tarleton, J., et al. “An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.” Hum Mol Genet, vol. 2, no. 11, Nov. 1993, pp. 1973–74. Pubmed, doi:10.1093/hmg/2.11.1973.
Tarleton J, Richie R, Schwartz C, Rao K, Aylsworth AS, Lachiewicz A. An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype. Hum Mol Genet. 1993 Nov;2(11):1973–1974.
Journal cover image

Published In

Hum Mol Genet

DOI

10.1093/hmg/2.11.1973

ISSN

0964-6906

Publication Date

November 1993

Volume

2

Issue

11

Start / End Page

1973 / 1974

Location

England

Related Subject Headings

  • Sequence Deletion
  • Repetitive Sequences, Nucleic Acid
  • RNA, Messenger
  • Phenotype
  • Male
  • Intellectual Disability
  • Infant
  • Humans
  • Genetics & Heredity
  • Fragile X Syndrome