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Results of search for 'au:"Werdani, Amina"'
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Authors
Ben Cheikh, Hassen
Ben Hamida, Nouha
Ben Mabrouk, Asma
Boussoffara, Raoudha
Driss, Nabil
Hasnaoui, Mehdi
Jerbi, Saida
Kerkeni, Emna
M'rad, Ridha
Mahjoub, Bahri
Sakka, Rania
Sfar, Mohamed Taher
Wannes, Selmen
Werdani, Amina
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Topics
Abnormalities, Multiple
Acute Disease
Child
Child, Preschool
Consanguinity
Craniofacial Abnormalities
Cross-Sectional Studies
DNA Mutational Analysis
Ethmoid Sinusitis
Exons
Female
Genotype
Growth Disorders
Humans
Male
Mutation
Neutropenia
Orbital Diseases
Phenotype
Tunisia
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English
Your search returned 2 results.
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1.
Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation.
[electronic resource]
by
Sakka, Rania
Mahjoub, Bahri
Kerkeni, Emna
Werdani, Amina
Boussoffara, Raoudha
Ben Cheikh, Hassen
M'rad, Ridha
Sfar, Mohamed Taher
Producer:
20190520
In:
Pediatric blood & cancer
vol. 65
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Available from publisher's website
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No items available.
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2.
Orbital complication of acute ethmoiditis: A Tunisian paediatric cross sectional study.
[electronic resource]
by
Ben Mabrouk, Asma
Wannes, Selmen
Hasnaoui, Mehdi
Werdani, Amina
Ben Hamida, Nouha
Jerbi, Saida
Driss, Nabil
Mahjoub, Bahri
Producer:
20200413
In:
American journal of otolaryngology
vol. 41
Online resources:
Available from publisher's website
Availability:
No items available.
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