Letters to the editor
- 1 July 1993
- journal article
- other
- Published by Elsevier in Human Immunology
- Vol. 37 (3) , 195-196
- https://doi.org/10.1016/0198-8859(93)90186-5
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Congenital 21-hydroxylase deficiency as a new deletion mutation: Detection in a proband during subsequent prenatal diagnosis by HLA typing and DNA analysisHuman Immunology, 1992
- Genomic Imprinting and Its Clinical ImplicationsNew England Journal of Medicine, 1992
- Uniparental disomy, isodisomy, and imprinting: Probable effects in man and strategies for their detectionAmerican Journal of Medical Genetics, 1991
- Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.Journal of Clinical Investigation, 1990
- Direct observation of the gene organization of the complement C4 and 21-hydroxylase loci by pulsed field gel electrophoresis.The Journal of Experimental Medicine, 1989
- A genetic linkage map of the human genomeCell, 1987
- A new genetic concept: Uniparental disomy and its potential effect, isodisomyAmerican Journal of Medical Genetics, 1980