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1 Ergebnisse
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GJB2 (connexin 26) gene mutations in Moroccan patients with..:
Abidi, Omar
;
Boulouiz, Redouane
;
Nahili, Halima
...
International Journal of Pediatric Otorhinolaryngology. 71 (2007) 8 - p. 1239-1245 , 2007
Link:
https://doi.org/10.1016/j.ijporl.2007.04.019
RT Journal T1
GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ijporl.2007.04.019&Exemplar=1&LAN=DE A1 Abidi, Omar A1 Boulouiz, Redouane A1 Nahili, Halima A1 Ridal, Mohammed A1 Alami, Mohamed Noureddine A1 Tlili, Abdelaziz A1 Rouba, Hassan A1 Masmoudi, Saber A1 Chafik, Abdelaziz A1 Hassar, Mohammed A1 Barakat, Abdelhamid PB Elsevier BV YR 2007 SN 0165-5876 JF International Journal of Pediatric Otorhinolaryngology VO 71 IS 8 SP 1239 OP 1245 LK http://dx.doi.org/https://doi.org/10.1016/j.ijporl.2007.04.019 DO https://doi.org/10.1016/j.ijporl.2007.04.019 SF ELIB - SuUB Bremen
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