TB and other respiratory infections

Citations 11-20 of 23 total displayed.

Electronic letters
CLCA1 gene polymorphisms in chronic obstructive pulmonary disease

A E Hegab, T Sakamoto, Y Uchida, A Nomura, Y Ishii, Y Morishima, M Mochizuki, T Kimura, W Saitoh, H H Massoud, H M Massoud, K M Hassanein, K Sekizawa
J. Med. Genet. 2004; 41: e27. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates

D Jeganathan, R Chodhari, M Meeks, O Færoe, D Smyth, K Nielsen, I Amirav, A S Luder, H Bisgaard, R M Gardiner, E M K Chung, H M Mitchison
J. Med. Genet. 2004; 41: 233-240. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation

A Iannaccone, D K Breuer, X F Wang, S F Kuo, E M Normando, E Filippova, A Baldi, S Hiriyanna, C B MacDonald, F Baldi, D Cosgrove, C C Morton, A Swaroop, M M Jablonski
J. Med. Genet. 2003; 40: e118. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

I Zito, S M Downes, R J Patel, M E Cheetham, N D Ebenezer, S A Jenkins, S S Bhattacharya, A R Webster, G E Holder, A C Bird, D E Bamiou, A J Hardcastle
J. Med. Genet. 2003; 40: 609-615. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasis

V N Ninis, M O Kylynç, M Kandemir, E Daðly, A Tolun
J. Med. Genet. 2003; 40: 530-535. [Extract] [Full text] [PDF] [Request Permissions] [ Publisher's Correction ]  

Electronic letters
Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies

E Petek, B Plecko-Startinig, C Windpassinger, H Egger, K Wagner, P M Kroisel
J. Med. Genet. 2003; 40: e47. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Streptococcal infection distinguishes different types of psoriasis

P Weisenseel, B Laumbacher, P Besgen, D Ludolph-Hauser, T Herzinger, M Roecken, R Wank, J C Prinz
J. Med. Genet. 2002; 39: 767-768. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
8p23 duplication reconsidered: is it a true euchromatic variant with no clinical manifestation?

C-H Tsai, S L Graw, L McGavran
J. Med. Genet. 2002; 39: 769-774. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
The phenotype of survivors of campomelic dysplasia

S Mansour, A C Offiah, S McDowall, P Sim, J Tolmie, C Hall
J. Med. Genet. 2002; 39: 597-602. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Atypical clinical picture of the Nijmegen breakage syndrome associated with developmental abnormalities of the brain

KRYSTYNA H CHRZANOWSKA, MARKUS STUMM, MONIKA BEKIESINSKA-FIGATOWSKA, RAYMONDA VARON, MAGDALENA BIALECKA, HANNA GREGOREK, JACEK MICHALKIEWICZ, MALGORZATA KRAJEWSKA-WALASEK, SERGIUSZ JOZWIAK, ANDRE REIS
J. Med. Genet. 2001; 38: e3. [Extract] [Full text] [PDF] [Request Permissions]