Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis

Author:

Willemsen Rob,Anar Burcu,Otero Yolanda De Diego,de Vries Bert B.A.,Hilhorst-Hofstee Yvonne,Smits Arie,van Looveren Eddy,Willems Patrick J.,Galjaard Hans,Oostra Ben A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Rapid fragile-X carrier screening and prenatal diagnosis using a nonradioactive PCR test;Brown;JAMA,1993

2. Evidence for the derivation of individual hair roots from three progenitor cells;Dancis;Hum Genet,1981

3. Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor;De Graaff;Am J Hum Genet,1995

4. Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey;De Vries;Am J Hum Genet,1997

5. Mental status of females with an FMR1 gene full mutation;De Vries;Am J Hum Genet,1996

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