Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

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Published in Hum Genet on September 01, 1988

Authors

G de Saint-Basile1, M C Bohler, A Fischer, J Cartron, J L Dufier, C Griscelli, S H Orkin

Author Affiliations

1: INSERM U 132, Hôpital des Enfants-Malades, Paris, France.

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