Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.

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 firs...

Description complète

Détails bibliographiques
Auteurs principaux: Tomlinson, I, Olschwang, S, Abelovitch, D, Nakamura, Y, Bodmer, W, Thomas, G, Markie, D
Format: Journal article
Langue:English
Publié: 1996