A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male

Page L. Sorensen, Kirin Basuta, Guadalupe Mendoza-Morales, Louise W. Gane, Andrea Schneider, Randi J Hagerman, Flora Tassone

Research output: Contribution to journalArticle

5 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1221-1224
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Volume158 A
Issue number5
DOIs
StatePublished - May 2012

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Fragile X Syndrome
DNA Methylation
Heterozygote
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. / Sorensen, Page L.; Basuta, Kirin; Mendoza-Morales, Guadalupe; Gane, Louise W.; Schneider, Andrea; Hagerman, Randi J; Tassone, Flora.

In: American Journal of Medical Genetics, Part A, Vol. 158 A, No. 5, 05.2012, p. 1221-1224.

Research output: Contribution to journalArticle

Sorensen, Page L. ; Basuta, Kirin ; Mendoza-Morales, Guadalupe ; Gane, Louise W. ; Schneider, Andrea ; Hagerman, Randi J ; Tassone, Flora. / A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. In: American Journal of Medical Genetics, Part A. 2012 ; Vol. 158 A, No. 5. pp. 1221-1224.
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