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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at risk.

Five pregnancies at risk for X-linked retinitis pigmentosa (RP) have been monitored by first-trimester prenatal diagnosis using DNA markers flanking the RP2 and RP3 loci. Three affected and two unaffected fetuses, including a female carrying a wild-type genotype, were predicted on the basis of marker segregation and estimation of the recombination fraction.[1]

References

  1. Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at risk. Iampieri, M.P., Mingarelli, R., Le Guern, E., Novelli, G., Dallapiccola, B. Prenat. Diagn. (1994) [Pubmed]
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