- Abstract:
-
Peutz-Jeghers' syndrome (PJS) is a disease with autosomal dominant inheritance, which is characterised by gastrointestinal hamartomata and characteristic melanin pigmentation. Three candidate sites for a PJS locus have recently been proposed, chromosomes 1p31-p32, 6q25 and 6p11-cen. At the first of these sites, a multipoint LOD score of 4.00 had been found, strongly suggesting genetic linkage to PJS. The last two candidate sites were suggested by the chromosomal breakpoints of a patient with ...
Expand abstract - Publisher copy:
- 10.1111/j.1469-1809.1996.tb00435.x
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- Journal:
- Annals of human genetics
- Volume:
- 60
- Issue:
- Pt 5
- Pages:
- 377-384
- Publication date:
- 1996-09-05
- DOI:
- EISSN:
-
1469-1809
- ISSN:
-
0003-4800
- URN:
-
uuid:616c9ef7-5aa0-4c3a-ac2b-8b9a615dbf54
- Source identifiers:
-
72310
- Local pid:
- pubs:72310
- Copyright date:
- 1996
Journal article
Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.
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