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

doi:10.1002/ajmg.a.35293

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 journal › Article

6 Scopus citations

Original language	English (US)
Pages (from-to)	1221-1224
Number of pages	4
Journal	American Journal of Medical Genetics, Part A
Volume	158 A
Issue number	5
DOIs	https://doi.org/10.1002/ajmg.a.35293
State	Published - May 2012

ASJC Scopus subject areas

Genetics(clinical)
Genetics

Cite this

Sorensen, P. L., Basuta, K., Mendoza-Morales, G., Gane, L. W., Schneider, A., Hagerman, R. J., & Tassone, F. (2012). A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. American Journal of Medical Genetics, Part A, 158 A(5), 1221-1224. https://doi.org/10.1002/ajmg.a.35293

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 journal › Article

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10.1002/ajmg.a.35293