| Literature DB >> 1979308 |
F P Cremers1, F Brunsmann, W Berger, E P van Kerkhoff, T J van de Pol, B Wieringa, I H Pawlowitzki, H H Ropers.
Abstract
In order to characterize a previously described submicroscopic deletion encompassing (part of) the choroideremia (tapetochoroidal dystrophy: TCD) gene, we have cloned a 10.5-kb EcoRI fragment from the patient's DNA; this fragment carries the junction between both deletion endpoints ("junction fragment"). The distal portion of this fragment defines a new marker within, or just distal to, the TCD gene. This marker has been employed to confirm the diagnosis in several affected family members, and to rule out carriership in a female at risk with conspicuous clinical signs.Entities:
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Year: 1990 PMID: 1979308 DOI: 10.1007/bf00205174
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132