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OA71 Le syndrome du canal carpien. Apport de l’echographie
by
Alouini-Mekki, R.
,
Allani, M.
,
Alouini, B.
,
Laadhari, H.
,
Bellara, I.
,
Ourteni, M.
,
Nikolova, N.
Published in
Journal de radiologie
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Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family
by
Chograni, M.
,
Alkuraya, F.S.
,
Ourteni, I.
,
Maazoul, F.
,
Lariani, I.
,
Chaabouni, H.B.
Published in
Clinical genetics
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La neuropathie autonome et déficit en vitamine D : quel lien ?
by
Hasni, Y.
,
Gueddas, M.
,
Ourteni, S.
,
Ben Amor, B.
,
El Fekih, H.
,
Ben Abdelkrim, A.
,
Kacem, M.
,
Chadli, M.
,
Maaroufi, A.
,
Ach, K.
Published in
Annales d'endocrinologie
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Annales D'endocrinologie
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Clinical Genetics
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Journal De Radiologie
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Adolescent
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Association
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Autosomal Recessive
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Cataract - Diagnosis
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Cataract - Genetics
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Cataracts
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Congenital Cataract
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Congenital Diseases
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Consanguinity
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Dna Mutational Analysis
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Echographie
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Female
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Genes, Recessive
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Genetic Disorders
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Genetics & Heredity
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Genome Scan
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Genotype & Phenotype
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Homozygote
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Humans
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Intellectual Disabilities
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Sciencedirect Journals
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Wiley-Blackwell Journals (Backfile Content)
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Wiley Online Library All Journals
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Bacon - Elsevier - Global Sciencedirect-Openaccess
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Elsevier
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Science Citation Index Expanded (Web Of Science)
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Wiley
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Free E-Journal (出版社公開部分のみ)
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