Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文（繁體）
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Language
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Tag
Find
Advanced
Familial spontaneous pneumotho...
Cite this
Text this
Email this
Print
Export Record
Export to RefWorks
Export to EndNoteWeb
Export to EndNote
Permanent link
Familial spontaneous pneumothorax and FBN1 mutations.
Bibliographic Details
Main Authors:
Cardy, C
,
Maskell, N
,
Handford, P
,
Arnold, A
,
Davies, R
,
Morrison, P
,
Thornley, P
Format:
Journal article
Language:
English
Published:
2004
Holdings
Description
Similar Items
Staff View
Similar Items
Familial spontaneous pneumothorax is not linked to FBN-1, the defective gene in the Marfan syndrome.
by: Maskell, N, et al.
Published: (2000)
Molecular analysis of eight mutations in FBN1.
by: Halliday, D, et al.
Published: (1999)
Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice.
by: Halliday, D, et al.
Published: (2002)
Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence.
by: Hutchinson, S, et al.
Published: (2001)
Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome
by: Aideen M. McInerney‐Leo, et al.
Published: (2020-03-01)