Cystic fibrosis and Young's syndrome (multiple letters) [2]

Lancet

Volumn 352, Issue 9133, 1998, Pages 1065-1066

  Pryor, J P ^a   Massie, J ^a   Wellesley, D ^a   Schwarz, M ^a  

^a LISTER HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE ION; ELECTROLYTE; FRUCTOSE; CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

AZOOSPERMIA; CASE REPORT; CLINICAL EXAMINATION; CYSTIC FIBROSIS; DIFFERENTIAL DIAGNOSIS; EPIDIDYMIS; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LETTER; MALE; PH; PRIORITY JOURNAL; SPERM; SWEAT TEST; VAS DEFERENS; YOUNG SYNDROME; GENETICS; MUTATION; NOTE; OLIGOSPERMIA; SYNDROME;

CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; MALE; MUTATION; OLIGOSPERMIA; SYNDROME;

EID: 0032569481     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0140-6736(05)60104-3     Document Type: Letter

References (5)

1. T Dork B Dworniczak C Aulehla-Scholz Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens Hum Genet 100 1997 365 377
2. B Costes E Girodon N Ghanem Frequent occurrence of the CFTR intron 8(TG)n 5T allele in men with congenital bilateral absence of the vas deferens Eur J Hum Genet 3(5) 1995 275 293
3. PF Pignatti C Bombieri M Benetazzo CFTR gene variant IVS8-5T in disseminated bronchiectasis Am J Hum Genet 58 1996 889 892
4. N Sharer M Schwarz G Malone Mutations in the cystic fibrosis gene in patients with chronic pancreatitis N Engl J Med 339 1998 645 652
5. PW Miller A Hamosh Macek M Jnr Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis Am J Hum Genet 59 1996 45 51