An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees
- 31 May 1996
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 67 (3) , 254-263
- https://doi.org/10.1002/(sici)1096-8628(19960531)67:3<254::aid-ajmg3>3.0.co;2-n
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23Nature Genetics, 1996
- Diagnostic Interview for Genetic StudiesArchives of General Psychiatry, 1994
- A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10Nature Genetics, 1993
- Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigreesNature Genetics, 1993
- Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22Science, 1992
- Risks of Affective Illness Among First-Degree Relatives of Bipolar I Old-Order Amish ProbandsArchives of General Psychiatry, 1992
- Bipolar affective disorders linked to DNA markers on chromosome 11Nature, 1987
- Best Estimate of Lifetime Psychiatric DiagnosisArchives of General Psychiatry, 1982
- Research Diagnostic CriteriaArchives of General Psychiatry, 1978
- A Danish Twin Study of Manic-Depressive DisordersThe British Journal of Psychiatry, 1977