Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("GARDNER, Phyllis")

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 4 of 4

  • Page / 1
Export

Selection :

  • and

Analysis of the Alternative Splicing of an FGFR2 Transcript Due to a Novel 5' Splice Site Mutation (1084+1 G>A): Case ReportTRAYNIS, Ilana; BERNSTEIN, Jonathan A; GARDNER, Phyllis et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 1, pp 104-108, issn 1055-6656, 5 p.Article

Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray : A new approach for newborn screening follow-upGARDNER, Phyllis; OITMAA, Eneli; MESSNER, Anna et al.Pediatrics (Evanston). 2006, Vol 118, Num 3, pp 985-994, issn 0031-4005, 10 p.Article

Novel contributions to the Asian CFTR mutation spectrum : Genotype and phenotype in Thai patients with cystic fibrosisSCHRIJVER, Iris; KARNSAKUL, Wikrom; LIMWONGSE, Chanin et al.American journal of medical genetics. 2005, Vol 133A, Num 1, pp 103-105, issn 0148-7299, 3 p.Article

A phase II, double-blind, randomized, placebo-controlled clinical trial of tgAAVCF using maxillary sinus delivery in patients with cystic fibrosis with antrostomiesWAGNER, John A; NEPOMUCENO, Ilynn B; GUGGINO, William B et al.Human gene therapy. 2002, Vol 13, Num 11, pp 1349-1359, issn 1043-0342Article

  • Page / 1