Defining the chromosomal basis of mental handicap
- 1 November 1999
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 354 (9191) , 1659-1660
- https://doi.org/10.1016/s0140-6736(99)00246-9
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Deletion of 22q11 in two brothers with different phenotypeAmerican Journal of Medical Genetics, 1998
- Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletionClinical Genetics, 1997
- Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphismsHuman Genetics, 1996
- The genetic basis for mental retardationQJM: An International Journal of Medicine, 1996
- Miller-Dieker SyndromeAmerican Journal of Diseases of Children, 1993
- DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASEThe Lancet, 1989