Frequency of inherited deletions of 22q11.
Open Access
- 1 September 1998
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 35 (9) , 789
- https://doi.org/10.1136/jmg.35.9.789
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
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- Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.Journal of Medical Genetics, 1993
- Rhodopsin mutations in autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa.British Journal of Ophthalmology, 1985