Authors: MEINDL A HOSENFELD D BRUCKL W SCHUFFENHAUER S JENDERNY J BACSKULIN A OPPERMANN HC SWENSSON O BOULOUX P MEITINGER T

Citation: A. Meindl et al., ANALYSIS OF A TERMINAL XP22.3 DELETION IN A PATIENT WITH 6 MONOGENIC DISORDERS - IMPLICATIONS FOR THE MAPPING OF X-LINKED OCULAR ALBINISM, Journal of Medical Genetics, 30(10), 1993, pp. 838-842