Archive ouverte UNIGE

Français
Search

 
Advanced search
Browse by...
  • Personal names
  • Academic structures
  • (0)Your selection
  • Latest additions
Deposit
  • Submit a document
  • Update a submission
Highlights
  • Generate a bibliography
  • Create an alert
  • My publisher's policy
  • Doctoral thesis
  • Restricted access masters
More informations
  • Manuals
  • Open Access & Copyright
  • UNIGE policies
  • Project history
  • Contacts
HomeAuthorsBouchardy, Isabelle

Bouchardy, Isabelle

 
  • Documents
  • Publications statistics
  • Export bibliography
 
Show items per page
Elements: 4
Page 1 on 1

2007

Scientific Articles

unige:8702
add to browser selection
MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous motherDayer, Alexandre; Bottani, Armand; Bouchardy, Isabelle; Fluss, Joel Victor; ... Morris, Michael Andréw

2006

Scientific Articles

unige:8741
add to browser selection
Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patientFarah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite

2003

Scientific Articles

unige:8937
add to browser selection
Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian familyNeerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw

2000

Scientific Articles

unige:27051
add to browser selection
Cystic fibrosis transmembrane conductance regulator does not affect neutrophil migration across cystic fibrosis airway epithelial monolayersPizurki, Lara Johanna; Morris, Michael Andréw; Chanson, Marc; Solomon, Melete; ... Suter, Susanne
add all | remove all
<< previous | | next >>
View all records: 68926
Back to top About Swiss Copyright
Validator | Admin