Molecular studies of the fragile X syndrome.

Molecular studies of the fragile X syndrome.

We have studied families segregating for the fragile X syndrome for the presence of amplification of the CGG repeat sequence adjacent to the HpaII Tiny Fragment (HTF) island in the FMR-1 gene. We demonstrate that 138/143 fragile X positive, mentally retarded males show a characteristic smear of frag...

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Hlavní autoři: Knight, S, Hirst, M, Roche, A, Christodoulou, Z, Huson, S, Winter, R, Fitchett, M, McKinley, M, Lindenbaum, R, Nakahori, Y
Médium: Journal article
Jazyk:English
Vydáno: 1992

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