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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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Peer Reviewed
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Molecular Genetics & Genomic Medicine
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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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Founder Haplotype
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Founder Mutation
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