Genetic screening / counselling

Citations 41-46 of 46 total displayed.

Review series
Genetics and respiratory disease  2: Alpha₁-antitrypsin deficiency, cirrhosis and emphysema

Ravi Mahadeva and David A Lomas
Thorax 1998; 53: 501-505. [Extract] [Full text] [PDF] [Request Permissions]  

Case reports
Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adult

D de Silva, A Osborne, SA Simpson, JC Dean, and A Seaton
Thorax 1998; 53: 149-150. [Abstract] [PDF] [Request Permissions]  

Editorials
Wheezing phenotypes in childhood

M Silverman and N Wilson
Thorax 1997; 52: 936-937. [PDF] [Request Permissions]  

Papers
Absence of genetic linkage of chromosome 5q31 with asthma and atopy in the general population

A Kamitani, ZY Wong, P Dickson, L van Herwerden, J Raven, AB Forbes, MJ Abramson, EH Walters, and SB Harrap
Thorax 1997; 52: 816-817. [Abstract] [PDF] [Request Permissions]  

Papers
Atopy phenotype in subjects with variants of the beta subunit of the high affinity IgE receptor

A Li and JM Hopkin
Thorax 1997; 52: 654-655. [Abstract] [PDF] [Request Permissions]  

Papers
Case of adults with cystic fibrosis has become an increasingly prominent part of the professional life of many respiratory physicians

DJ Shale
Thorax 1997; 52: 95-96. [PDF] [Request Permissions]