يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"Abdelhak, Ahlem"', وقت الاستعلام: 1.11s تنقيح النتائج
  1. 1
    دورية أكاديمية
    High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis

    المؤلفون: 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

    المصدر: Molecular Genetics & Genomic Medicine ; volume 2, issue 2, page 160-165 ; ISSN 2324-9269 2324-9269

    الإتاحة: https://doi.org/10.1002/mgg3.55Test

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  2. 2
    دورية أكاديمية
    High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

    المؤلفون: 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

    المساهمون: Département d'Histologie et de Cytogénétique - Institut Pasteur de Tunis, Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Department of tumor biology, Institut Curie Paris, Hedi Chaker Hospital Sfax (CHU Sfax), Department of Haematology and Transplantation, National Bone Marrow Transplantation Centre, Department of Peadiatric Immuno-Haematology, National Bone Marrow Transplantation, Haematology Department, Aziza Othmana Hospital, Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM), Université Sorbonne Paris Cité (USPC), Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Pediatrics, Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), This study was supported by the Tunisian Ministry of Higher Education and Scientific Research (Laboratory of “Biomedical Genomics and Oncogenetics” LR11IPT05) and by the Tunisian Ministry of Health., The Tunisian Fanconi Anemia Study Group

    المصدر: ISSN: 2324-9269 ; Molecular Genetics and Genomic Medicine ; https://riip.hal.science/pasteur-01098539Test ; Molecular Genetics and Genomic Medicine, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩.

    مصطلحات موضوعية: Exon 15 deletion, Fanconi anemia, founder haplotype, founder mutation, MLPA, [SDV]Life Sciences [q-bio], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24689079; pasteur-01098539; https://riip.hal.science/pasteur-01098539Test; https://riip.hal.science/pasteur-01098539/documentTest; https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest; PUBMED: 24689079; PUBMEDCENTRAL: PMC3960058

    الإتاحة: https://doi.org/10.1002/mgg3.55Test
    https://riip.hal.science/pasteur-01098539Test
    https://riip.hal.science/pasteur-01098539/documentTest
    https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest

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  3. 3
    دورية أكاديمية
    High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

    المؤلفون: 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

    المساهمون: Département d'Histologie et de Cytogénétique - Institut Pasteur de Tunis, Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Department of tumor biology, Institut Curie Paris, Hedi Chaker Hospital Sfax, Department of Haematology and Transplantation, National Bone Marrow Transplantation Centre, Department of Peadiatric Immuno-Haematology, National Bone Marrow Transplantation, Haematology Department, Aziza Othmana Hospital, Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM), Université Sorbonne Paris Cité (USPC), Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Pediatrics, Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), This study was supported by the Tunisian Ministry of Higher Education and Scientific Research (Laboratory of “Biomedical Genomics and Oncogenetics” LR11IPT05) and by the Tunisian Ministry of Health., The Tunisian Fanconi Anemia Study Group

    المصدر: ISSN: 2324-9269 ; Molecular Genetics and Genomic Medicine ; https://riip.hal.science/pasteur-01098539Test ; Molecular Genetics and Genomic Medicine, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩.

    مصطلحات موضوعية: Exon 15 deletion, Fanconi anemia, founder haplotype, founder mutation, MLPA, [SDV]Life Sciences [q-bio], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24689079; pasteur-01098539; https://riip.hal.science/pasteur-01098539Test; https://riip.hal.science/pasteur-01098539/documentTest; https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest; PUBMED: 24689079; PUBMEDCENTRAL: PMC3960058

    الإتاحة: https://doi.org/10.1002/mgg3.55Test
    https://riip.hal.science/pasteur-01098539Test
    https://riip.hal.science/pasteur-01098539/documentTest
    https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest

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  4. 4
    دورية أكاديمية
    High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

    المؤلفون: 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

    المساهمون: Département d'Histologie et de Cytogénétique - Institut Pasteur de Tunis, Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Department of tumor biology, Institut Curie Paris, Hedi Chaker Hospital Sfax, Department of Haematology and Transplantation, National Bone Marrow Transplantation Centre, Department of Peadiatric Immuno-Haematology, National Bone Marrow Transplantation, Haematology Department, Aziza Othmana Hospital, Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM), Université Sorbonne Paris Cité (USPC), Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Pediatrics, Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), This study was supported by the Tunisian Ministry of Higher Education and Scientific Research (Laboratory of “Biomedical Genomics and Oncogenetics” LR11IPT05) and by the Tunisian Ministry of Health., The Tunisian Fanconi Anemia Study Group

    المصدر: ISSN: 2324-9269 ; Molecular Genetics and Genomic Medicine ; https://riip.hal.science/pasteur-01098539Test ; Molecular Genetics and Genomic Medicine, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩.

    مصطلحات موضوعية: Exon 15 deletion, Fanconi anemia, founder haplotype, founder mutation, MLPA, [SDV]Life Sciences [q-bio], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24689079; pasteur-01098539; https://riip.hal.science/pasteur-01098539Test; https://riip.hal.science/pasteur-01098539/documentTest; https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest; PUBMED: 24689079; PUBMEDCENTRAL: PMC3960058

    الإتاحة: https://doi.org/10.1002/mgg3.55Test
    https://riip.hal.science/pasteur-01098539Test
    https://riip.hal.science/pasteur-01098539/documentTest
    https://riip.hal.science/pasteur-01098539/file/mgg30002-0160.pdfTest

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    أضف إلى المفضلة
  5. 5
    دورية أكاديمية
    High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

    المؤلفون: 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

    المساهمون: Département d'Histologie et de Cytogénétique - Institut Pasteur de Tunis, Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Department of tumor biology, Institut Curie Paris, Hedi Chaker Hospital Sfax, Department of Haematology and Transplantation, National Bone Marrow Transplantation Centre, Department of Peadiatric Immuno-Haematology, National Bone Marrow Transplantation, Haematology Department, Aziza Othmana Hospital, Unité de génétique et biologie des cancers (U830), Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5), Université Sorbonne Paris Cité (USPC), Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Pediatrics, Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), This study was supported by the Tunisian Ministry of Higher Education and Scientific Research (Laboratory of “Biomedical Genomics and Oncogenetics” LR11IPT05) and by the Tunisian Ministry of Health., The Tunisian Fanconi Anemia Study Group

    المصدر: ISSN: 2324-9269 ; Molecular Genetics and Genomic Medicine ; https://hal-riip.archives-ouvertes.fr/pasteur-01098539Test ; Molecular Genetics and Genomic Medicine, Wiley, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩.

    مصطلحات موضوعية: MLPA, Fanconi anemia, founder haplotype, founder mutation, Exon 15 deletion, [SDV]Life Sciences [q-bio], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24689079; pasteur-01098539; https://hal-riip.archives-ouvertes.fr/pasteur-01098539Test; https://hal-riip.archives-ouvertes.fr/pasteur-01098539/documentTest; https://hal-riip.archives-ouvertes.fr/pasteur-01098539/file/mgg30002-0160.pdfTest; PUBMED: 24689079; PUBMEDCENTRAL: PMC3960058

    الإتاحة: https://doi.org/10.1002/mgg3.55Test
    https://hal-riip.archives-ouvertes.fr/pasteur-01098539Test
    https://hal-riip.archives-ouvertes.fr/pasteur-01098539/documentTest
    https://hal-riip.archives-ouvertes.fr/pasteur-01098539/file/mgg30002-0160.pdfTest

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    أضف إلى المفضلة
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