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1
المؤلفون: Hanene Hannachi, Inesse Ben Abdallah Bouhjar, Soumaya Mougou-Zrelli, Ali Saad, Abir Gmidène, Naoufel Gadour, Hatem Elghezal, Imed Harrabi, Najla Soyah
المصدر: Journal of Pediatric Genetics. :175-180
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, education.field_of_study, business.industry, Population, Cytogenetics, Karyotype, Congenital malformations, medicine.disease, Article, Epilepsy, Pediatrics, Perinatology and Child Health, Intellectual disability, medicine, Etiology, education, business, Genetics (clinical), Non syndromic
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2
المؤلفون: Hannachi Hanene, Ali Saad, Najla Soyah, Abir Gmidène, Hatem Elghezal, Soumaya Mougou, Inesse Ben Abdallah Bouhjar
المصدر: Journal of pediatric genetics. 1(1)
مصطلحات موضوعية: Genetics, medicine.diagnostic_test, Marker chromosome, Ring chromosome, Biology, medicine.disease, Hypotonia, Article, Pediatrics, Perinatology and Child Health, Tetrasomy, Speech delay, Chromosomal region, medicine, medicine.symptom, Trisomy, Genetics (clinical), Fluorescence in situ hybridization
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3
المؤلفون: Inesse Ben Abdallah Bouhjar, Hela Ben Khelifa, Najla Soyah, Soumaya Mougou Zerrelli, Moez Gribaa, Hatem Elghezal, Ali Saad, null Prf: Tunisian Network on Mental Ret
المصدر: International Journal of Human Genetics. 12:157-171
مصطلحات موضوعية: Genetics, Genetics (clinical)
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4
المؤلفون: Inesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Ali Saad, Hatem Elghezal, Moez Gribaa, Soumaya Mougou, Abir Gmidène, Damien Sanlaville, Audrey Labalme, Najla Soyah
المصدر: European Journal of Medical Genetics. 55:461-465
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Chromosomal translocation, Biology, Chromosome Duplication, Gene duplication, Genetics, medicine, Humans, In Situ Hybridization, Fluorescence, Genetics (clinical), X chromosome, Oligonucleotide Array Sequence Analysis, Chromosomes, Human, X, Comparative Genomic Hybridization, Infant, Newborn, Chromosome, Karyotype, General Medicine, Hypotonia, Chromosome 3, Child, Preschool, Muscle Hypotonia, Chromosomes, Human, Pair 3, Chromosome Deletion, medicine.symptom, Prader-Willi Syndrome, Comparative genomic hybridization
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5
المؤلفون: Yasser Hassen Babair, Hatem Elghezal, Samia Sobki, Amal Al Hashem, Brahim Tabarki, Inesse Ben-Abdallah-Bouhjar
المصدر: Journal of Genetic Disorders & Genetic Reports.
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, medicine.diagnostic_test, business.industry, medicine.disease, Severe expressive language delay, Gene duplication, Speech delay, Intellectual disability, medicine, Tandem exon duplication, medicine.symptom, business, Hydronephrosis, Fluorescence in situ hybridization, Comparative genomic hybridization
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6
المؤلفون: Ryma Gritly, Ali Saad, Soumaya Mougou-Zerelli, Hela Ben Khelifa, Hatem Elghezal, Inesse Ben-Abdallah-Bouhjar, Najla Soyah, Damien Sanlaville
المصدر: Gene. 527(2)
مصطلحات موضوعية: Male, Candidate gene, Ichthyosis, X-Linked, Adolescent, Non-allelic homologous recombination, Biology, Genetics, Steroid sulfatase, medicine, Humans, X chromosome, In Situ Hybridization, Fluorescence, Chromosomes, Human, X, Comparative Genomic Hybridization, X-linked ichthyosis, Ichthyosis, Genetic disorder, Nuclear Proteins, General Medicine, medicine.disease, FMR1, Pedigree, Mental Retardation, X-Linked, Female, Steryl-Sulfatase, Chromosome Deletion
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7
المؤلفون: Mouna Turki, Fatma Kamoun, Kamel Jamoussi, Foued Haj Salama, Abdelhedi Miled, Fahmi Nasrallah, Ali Saad, Habiba Chaabouni, Meriam Messeddi, Ahmed Sahloul Essoussi, Ben Dridi, Soumaya Mougou, M. Chaabouni, Henda Chahed, Elyes Chabchoub, Haifa Sanhaji, Hatem Elghezal, Houda Ben Othman, Faouzi Maaloul, Hela Ben Khelifa, Hassen Kamoun, E. Ellouz, Inesse Ben Abdallah Bouhjar, Salima Ferchichi, Jihene Bouguila, Marie Françoise, A. Achour, Hend Ben Khelifa, Lamia Ben Jemaa, Fatma Ayedi, Ramzi Zemni, Moez Gribaa, Lamia Boughamoura
المصدر: INTERNATIONAL JOURNAL OF HUMAN GENETICS. 12
مصطلحات موضوعية: Genetics, Candidate gene, medicine.diagnostic_test, Chromosomal translocation, Karyotype, Biology, Subtelomere, medicine.disease, Gene duplication, Intellectual disability, Genotype, medicine, Genetics (clinical), Fluorescence in situ hybridization
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8
المؤلفون: Abir Gmidène, Audrey Labalme, Hanane Hannachi, Inesse Ben Abdallah Bouhjar, Sonia Missaoui, Najla Soyah, Hatem Elghezal, Ali Saad, Damien Sanlaville, Soumaya Mougou Zerelli
المصدر: American journal of medical genetics. Part A. (7)
مصطلحات موضوعية: Genetics, Male, medicine.medical_specialty, Comparative Genomic Hybridization, Chromosomes, Human, Pair 22, Cytogenetics, Chromosome, Chromosomal translocation, Karyotype, Trisomy, Biology, medicine.disease, Developmental disorder, Phenotype, Intellectual Disability, Gene duplication, medicine, Humans, Child, Chromosomes, Human, Pair 9, Genetics (clinical), Comparative genomic hybridization
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9
المؤلفون: Inesse Ben Abdallah Bouhjar
المصدر: Pediatric Neurology. 47:74-75
مصطلحات موضوعية: Developmental Neuroscience, Neurology, Pediatrics, Perinatology and Child Health, Neurology (clinical)