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Showing 1 to 1 of 1 for “"chromosome haplotype"”.

  1. Analisi molecolare in pazienti italiani con sindrome di Lowe

    … phenotype of Lowe syndrome in a female. The X chromosome inactivation studies detected an extremely skewed inactivation pattern with a ratio of 100:0 in the propositus as well as in five out of seven unaffected female relatives in four generations. The OCRL1 "de novo" mutation resides in the …

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