Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2

The Coffin-Lowry syndrome (CLS) is an X-linked inherited disease of unknown pathogenesis characterized by severe mental retardation, typical facial and digital anomalies, and progressive skeletal deformations. Our previous linkage analysis, based on four pedigrees with the disease, suggested a local...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Biancalana, V., Briard, M. L., David, A., Gilgenkrantz, S., Kaplan, J., Mathieu, M., Piussan, C., Poncin, J., Schinzel, A., Oudet, C., Hanauer, A.
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682597/
https://ncbi.nlm.nih.gov/pubmed/1349200
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki