Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome (Q28273791)
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Current Data About Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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(P1476) "Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome" (language: en)
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(P2093) A J Verkerk
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M Pieretti
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Y H Fu
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D P Kuhl
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S Richards
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M F Victoria
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F P Zhang
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External Links
(P356) 10.1016/0092-8674(91)90397-H
(P698) 1710175
(P3181) 559017