Linkage homogeneity near the fragile X locus in normal and fragile X families
- 1 July 1991
- Vol. 10 (3) , 576-582
- https://doi.org/10.1016/0888-7543(91)90438-k
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomePublished by Elsevier ,2004
- Linkage heterogeneity and fragile XHuman Genetics, 1988
- Multilocus analysis of the fragile X syndromeHuman Genetics, 1988
- Genetic heterogeneity of X-linked mental retardation with fragile X Association of tight linkage to factor IX and incomplete penetrance in malesAnnals of Human Genetics, 1987
- Further evidence for genetic heterogeneity in the fragile X syndromeHuman Genetics, 1987
- DNA linkage studies in the fragile X syndrome suggest genetic heterogeneityAmerican Journal of Medical Genetics, 1986
- Genetic linkage heterogeneity in the fragile X syndromeHuman Genetics, 1985
- Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)Human Genetics, 1985
- LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBEThe Lancet, 1984
- Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal maleNature, 1983