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2 research outputs found
Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome
Author
A Pandya
A Pfenniger
+22Â more
A Wonkam
Ambroise Wonkam
AY Jan
BA Skinner
Collet Dandara
EA de Zwart-Storm
EJ Barker
G Richard
G Richard
Geneviève Bengono Toure
I Todt
J Mazereeuw-Hautier
Jason Bosch
Jean Jacques N Noubiap
L Jonard
L Maintz
RI Kabahuma
S Iossa
T Lazic
WH Evans
WX Zong
XZ Liu
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
Full text link
Crossref
Aetiology of childhood hearing loss in Cameroon (sub-Saharan Africa)
Author
Ambroise Wonkam
Bamiou
+33Â more
Bengono
Bowen
Brobby
Brown
Bureau international d’audiophonologie
Cohen
Fay
Fisch
François Djomou
Fraser
Geneviève Bengono Toure
Gray
Ijaduola
Jean Jacques N. Noubiap
Karen Fieggen
Li
Mafong
McPherson
Mondain
Olusanya
Paparella
Reyes
Riazuddin
Richard
Richard Njock
Stevenson
Tarabichi
The World Bank
Trotta
Wonkam
Wright
Wu
Yuan
Publication venue
'Elsevier BV'
Publication date
Field of study
No full text
Crossref