Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24–25

Por Geremek, M, Ziętkiewicz, E, Diehl, S R, Alizadeh, B Z, Wijmenga, C, Witt, M
Publicado em 2006

RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa

Por Moore, A, Escudier, E, Roger, G, Tamalet, A, Pelosse, B, Marlin, S, Clément, A, Geremek, M, Delaisi, B, Bridoux, A‐M, Coste, A, Witt, M, Duriez, B, Amselem, S
Publicado em 2006