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- W2093322414 abstract "We report a female infant born to a mother with incontinentia pigmenti (IP) and a father with haemophilia A, who manifests both disorders. Analysis of peripheral blood DNA from the infant, her mother, and two female relatives with IP showed a highly skewed pattern of X inactivation. Random patterns were observed in the infant9s two sisters, who do not have IP and have normal carrier activity of factor VIII. Preferential inactivation of the X chromosome bearing the IP mutation, probably by negative selection, appears to have unmasked the factor VIII mutation on the infant9s other X chromosome. This illustrates an unusual mechanism for the manifestation of an X linked disease in a heterozygous female." @default.
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- W2093322414 title "Interaction of incontinentia pigmenti and factor VIII mutations in a female with biased X inactivation, resulting in haemophilia." @default.
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- W2093322414 doi "https://doi.org/10.1136/jmg.30.6.497" @default.
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