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Search Results - Othmen, Tarek B.
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High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis
by
Amouri, Ahlem
,
Talmoudi, Faten
,
Messaoud, Olfa
,
d'Enghien, Catherine D.
,
Rekaya, Mariem B.
,
Allegui, Ines
,
Azaiez, Héla
,
Kefi, Rym
,
Abdelhak, Ahlem
,
Meseddi, Sondes H.
,
Torjemane, Lamia
,
Ouederni, Monia
,
Mellouli, Fethi
,
Abid, Héla B.
,
Aissaoui, Lamia
,
Bejaoui, Mohamed
,
Othmen, Tarek B.
,
Lyonnet, Dominique S.
,
Soulier, Jean
,
Hachicha, Mongia
,
Dellagi, Koussay
,
Abdelhak, Sonia
Published in
Molecular genetics & genomic medicine
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High frequency of exon 15 deletion in the FANCA gene in T unisian patients affected with F anconi anemia disease: implication for diagnosis
by
Amouri, Ahlem
,
Talmoudi, Faten
,
Messaoud, Olfa
,
d'Enghien, Catherine D.
,
Rekaya, Mariem B.
,
Allegui, Ines
,
Azaiez, Héla
,
Kefi, Rym
,
Abdelhak, Ahlem
,
Meseddi, Sondes H.
,
Torjemane, Lamia
,
Ouederni, Monia
,
Mellouli, Fethi
,
Abid, Héla B.
,
Aissaoui, Lamia
,
Bejaoui, Mohamed
,
Othmen, Tarek B.
,
Lyonnet, Dominique S.
,
Soulier, Jean
,
Hachicha, Mongia
,
Dellagi, Koussay
,
Abdelhak, Sonia
Published in
Molecular genetics & genomic medicine
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Depth of Response to ≥VGPR at Completion of Induction Influences Outcome Post ASCT, on Behalf of the Tunisian Myeloma Study Group
by
Mansouri, Raoudha
,
El fatmi, Rim
,
Ghédira, Héla
,
Kallel, Faten
,
Ben Abdejelil, Nour
,
Zahra, Kmira
,
Ben Romdhane, Neila
,
Kéfi, Salma
,
Medhaffer, Moez
,
Manai, Zeineb
,
Ben Sayed, Nesrine
,
Bchir, Manel
,
Zarrouk, Mohamed
,
Zriba, Sami
,
Boukhris, Sarra
,
Safra, Ines
,
Meddeb, Mounira
,
Laatiri, Adnene
,
Elloumi, Moez
,
M'Sadek, Fehmi
,
Khélif, Abderrahmen
,
Meddeb, Balkis
,
Leleu, Xavier
,
Ben Othmen, Tarek
Published in
Blood
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Molecular Genetics & Genomic Medicine
2 results
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Blood
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Subjects
Diagnosis
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Genetic Counseling
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Haplotypes
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Mutation
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Analysis
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Anemia
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Bone Marrow
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Bone Marrow Transplantation
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Consanguinity
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Deoxyribonucleic Acid
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Dna
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Exon 15 Deletion
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Family
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Fanca Gene
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Fanconi Anemia
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Fanconi Syndrome
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Fanconi's Anemia
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Founder Effect
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