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Amina Bakhchane
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Amina Bakhchane
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Amina Bakhchane
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1
Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
by
Zineb Kindil
,
Mohamed Amine Senhaji
,
Amina
Bakhchane
,
Hicham Charoute
,
Soumia Chihab
,
Sellama Nadifi
,
Abdelhamid Barakat
Published 2017-12-01
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Article
2
Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.
by
Amina
Bakhchane
,
Majida Charif
,
Sara Salime
,
Redouane Boulouiz
,
Halima Nahili
,
Rachida Roky
,
Guy Lenaers
,
Abdelhamid Barakat
Published 2015-01-01
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Article
3
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
by
Amina
Bakhchane
,
Majida Charif
,
Amale Bousfiha
,
Redouane Boulouiz
,
Halima Nahili
,
Hassan Rouba
,
Hicham Charoute
,
Guy Lenaers
,
Abdelhamid Barakat
Published 2017-01-01
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Article
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