(Q33679734)
Statements
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Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus (English)
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M Losekoot
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E Hoogendoorn
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R Olmer
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C C Jansen
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J C Oosterwijk
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A M van den Ouweland
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D J Halley
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S T Warren
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R Willemsen
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B A Oostra
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E Bakker
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1 November 1997
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924-926
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Identifiers
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