المؤلفون: Hatem Elghezal

المصدر: Journal of Biochemical and Clinical Genetics, Vol 5, Iss 2, Pp 35-36 (2022)

مصطلحات موضوعية: na, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.ejmanager.com/fulltextpdf.php?mno=66817; https://doaj.org/toc/1658-807X

URL الوصول: https://doaj.org/article/8d11910611224596a5a053634d91014c

المؤلفون: Nawaf Alkhayat, Ghaleb Elyamany, Yasser Elborai, Qanita Sedick, Mohammad Alshahrani, Omar Al Sharif, Abdulmalik Alenezy, Amjad Hammdan, Hatem Elghezal, Omar Alsuhaibani, Mansour S. Aljabry, May AlMoshary, Eman Al Mussaed

المصدر: Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-11 (2019)

مصطلحات موضوعية: Acute leukemia, Rare chromosomal abnormalities, Outcome, Pediatric, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13039-019-0454-0; https://doaj.org/toc/1755-8166

URL الوصول: https://doaj.org/article/b55d7fca52f44ddebb9ef81726568a3e

المؤلفون: Nawaf Alkhayat, Yasser Elborai, Omer Al Sharif, Mohammad Al Shahrani, Omar Alsuhaibani, Mohammed Awad, Hatem Elghezal, Inesse ben-abdallah Bouhajar, Mona Alfaraj, Eman Al Mussaed, Fahad Alabbas, Ghaleb Elyamany

المصدر: Clinical Medicine Insights: Oncology, Vol 11 (2017)

مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1179-5549

URL الوصول: https://doaj.org/article/211e9ee9ac7e4d9b9d263231b26114c2

المؤلفون: Ghaleb Elyamany, Kamal Fadalla, Hatem Elghezal, Omar Alsuhaibani, Hani Osman, Abdulaziz Al-Abulaaly

المصدر: Clinical Medicine Insights: Pathology, Vol 2014, Iss 7, Pp 21-27 (2014)

مصطلحات موضوعية: Pathology, RB1-214

وصف الملف: electronic resource

Relation: http://www.la-press.com/chronic-lymphocytic-leukemia-with-t1418q32q21-as-a-sole-cytogenetic-ab-article-a4400; https://doaj.org/toc/1179-5557

URL الوصول: https://doaj.org/article/6c798222ab00434aa847ddb370cceccb

المؤلفون: Sana Bouraoui, Soumaya Mougou, Afef Drira, Faten Tabka, Nouha Bouali, Najib Mrizek, Hatem Elghezal, Ali Saad

المصدر: International Journal of Occupational Medicine and Environmental Health, Vol 26, Iss 1, Pp 144-154 (2013)

مصطلحات موضوعية: centromere-micronucleus assay, occupational radiation exposure, hospital workers, centromere negative micronuculei, Medicine

وصف الملف: electronic resource

Relation: http://ijomeh.eu/A-cytogenetic-approach-to-the-effects-of-low-levels-of-ionizing-radiation-ir-on-the-exposed-tunisian-hospital-workers,2222,0,2.html; https://doaj.org/toc/1232-1087; https://doaj.org/toc/1896-494X

URL الوصول: https://doaj.org/article/721573aa5dbd4533a1733b644e913ca4

المؤلفون: Ghaleb Elyamany, Ali Matar Alzahrani, Eman Al Mussaed, Hassan Aljasem, Sultan Alotaibi, Hatem Elghezal

المصدر: Case Reports in Hematology, Vol 2015 (2015)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2090-6560; https://doaj.org/toc/2090-6579

URL الوصول: https://doaj.org/article/49634086d3bf45a0ba091ed5ea0e105b

المؤلفون: Abir Gmidène, Hatem Elghezal, Hlima Sennana, Yosra Ben Youssef, Balkiss Meddeb, Moez Elloumi, Abderrahim Khlif, Ali Saad

المصدر: Advances in Hematology, Vol 2009 (2009)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1687-9104; https://doaj.org/toc/1687-9112

URL الوصول: https://doaj.org/article/05646d84e6c84e1fb51ae403e123b25b

المؤلفون: Amal Alhashem, Saria Alazmeh, Ayla Barakat, Ahmed Alfares, Hatem Elghezal

المصدر: J Pediatr Genet

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Renal ectopia, business.industry, Ring chromosome, Chromosomal disorder, Variable presentation, medicine.disease, Short stature, Café au lait spot, Pediatrics, Perinatology and Child Health, Speech delay, medicine, medicine.symptom, Presentation (obstetrics), business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090e67ca72da3721234ff9df4acc7d67
https://doi.org/10.1055/s-0040-1721135

المؤلفون: Lakhal, Besma, Ben-Hadj-Khalifa, Sonia, Bouali, Nouha, Braham, Rim, Hatem, Elghezal, Saad, Ali

المصدر: Gene ; volume 526, issue 2, page 498 ; ISSN 0378-1119

الاتاحة: https://doi.org/10.1016/j.gene.2013.04.001
https://api.elsevier.com/content/article/PII:S0378111913004162?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0378111913004162?httpAccept=text/plain

المؤلفون: Ayesh Almazyad, Abdullah Al Jasser, Amal Alhashem, Omar Alsuhaibani, Ahmed Alfares, Khowla Alfayez, Inesse Ben Abdallah, Hatem Elghezal, Nasser Almobadel

المصدر: European journal of medical genetics. 64(7)

مصطلحات موضوعية: Male, Ring chromosome, Pseudoautosomal region, Chromosome Disorders, Biology, Short stature, Short Stature Homeobox Protein, Gene Duplication, Turner syndrome, Gene duplication, Genetics, medicine, Humans, Ring Chromosomes, Genetics (clinical), X chromosome, Chromosomes, Human, X, Hypospadias, Karyotype, General Medicine, Syndrome, medicine.disease, Child, Preschool, Microcephaly, medicine.symptom, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0fb9f4ec64e7eb7e09dd986905147b
https://pubmed.ncbi.nlm.nih.gov/33872775

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fdad86779d711d3d171339b2f6bf85c
https://doi.org/10.3233/pge-2012-027

المؤلفون: Nawaf, Alkhayat, Yasser, Elborai, Omer, Al Sharif, Mohammad, Al Shahrani, Omar, Alsuhaibani, Mohammed, Awad, Hatem, Elghezal, Inesse, Ben-Abdallah Bouhajar, Mona, Alfaraj, Eman, Al Mussaed, Fahad, Alabbas, Ghaleb, Elyamany

المصدر: Clinical Medicine Insights. Oncology

مصطلحات موضوعية: outcome, acute lymphoblastic leukemia, FLT3, cytogenetic abnormalities, Original Research

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::f39adc853e6c4780cc66f06a6048afb1
https://pubmed.ncbi.nlm.nih.gov/28811744

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7f15b9c08c5eaaeeeb41f02689c2ce3
https://pubmed.ncbi.nlm.nih.gov/27625804

المؤلفون: Stefan J. White, Marc Fellous, Besma Lakhal, Peter Koopman, Diego A. Ojeda, Hanène Landolsi, Dora Janeth Fonseca, Sonia Grover, Ali Saâd, Hatem Elghezal, Carlos Martín Restrepo, Margaret Zacharin, Stefanie Eggers, Paul Laissue, Garry L. Warne, Alexandra C. Nevin Lam, Rim Braham, Andrew H. Sinclair, Erin Turbitt

المصدر: Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

مصطلحات موضوعية: Nonsynonymous substitution, endocrine system diseases, DNA Mutational Analysis, Gene sequence, Primary Ovarian Insufficiency, Gene mutation, medicine.disease_cause, Gene, Pathogenesis, Computer model, Gene duplication, Female fertility, Cbp/p300 interacting transactivator with ed rich tail 2 gene, Priority journal, Mutation, Genetic analysis, General Medicine, Open reading frame, Middle Aged, female genital diseases and pregnancy complications, Premature ovarian failure, Female, Human, Adult, medicine.medical_specialty, Major clinical study, Biology, Article, Disease association, Idiopathic disease, Physiology (medical), Internal medicine, medicine, Humans, Human tissue, Gene amplification, Biochemistry (medical), Public Health, Environmental and Occupational Health, Case-control study, Mutational analysis, medicine.disease, Repressor Proteins, Endocrinology, Case-Control Studies, Genetic association, Trans-Activators, Genetic variability, Controlled study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48cf55360cd60b1b9126a996f42c542b
https://doi.org/10.1016/j.trsl.2012.05.006

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)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::13b8345d39d8c8bdeb006041feee232d
https://doi.org/10.1080/09723757.2012.11886178

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::627d7ec59f292275b8f627320ee7ddb5
https://doi.org/10.1016/j.ejmg.2012.04.011

المؤلفون: Sonia Abdelhak, Ahlem Amouri, Lamia Aissaoui, Koussay Dellagi, Mounir Frikha, Hatem Bellaaj, Hatem Elghezal, H Ben Abid, S Hammemi, Lamia Torjemane, le Groupe d’étude tunisien de l’anémie de Fanconi Getaf, Mohamed Bejaoui, Y Ben Youssef, Mongia Hachicha, S. Hadiji Mseddi, Monia Ouederni, F Telmoudi, T Ben Othmen, Lobna Kammoun, Y. Ben Abdennebi

المصدر: Archives de Pédiatrie. 19:467-475

مصطلحات موضوعية: Gynecology, medicine.medical_specialty, business.industry, Pediatrics, Perinatology and Child Health, Medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3da2f65142df715c4eaa3fe3c45edc10
https://doi.org/10.1016/j.arcped.2012.02.017

المؤلفون: Hanène Landolsi, Meriem Mehdi, Soumaya Mougou, Sonia Brahem, Ali Saad, Hatem Elghezal

المصدر: Urology. 78:792-796

مصطلحات موضوعية: Adult, Male, Abortion, Habitual, endocrine system, DNA damage, Urology, media_common.quotation_subject, Semen, Fertility, DNA Fragmentation, Andrology, Pregnancy, Recurrence, In Situ Nick-End Labeling, medicine, Humans, Sperm motility, media_common, urogenital system, business.industry, Case-control study, Middle Aged, medicine.disease, Spermatozoa, Sperm, Case-Control Studies, Karyotyping, Sperm Motility, DNA fragmentation, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::276e3ce69141c61da7ff62b70abe9d6f
https://doi.org/10.1016/j.urology.2011.05.049

المؤلفون: Hatem Elghezal, Mehdi Jerbi, Soumaya Mougou-Zerelli, Mounir Ajina, Ali Saad, Sonia Brahem, Molka Kammoun

المصدر: Journal of Assisted Reproduction and Genetics. 28:971-977

مصطلحات موضوعية: Adult, Male, endocrine system, Aneuploidy, Semen, Semen analysis, Biology, urologic and male genital diseases, Andrology, Genetics, medicine, Humans, In patient, In Situ Hybridization, Fluorescence, reproductive and urinary physiology, Genetics (clinical), Chromosomes, Human, X, Chromosomes, Human, Y, medicine.diagnostic_test, urogenital system, Obstetrics and Gynecology, Oligospermia, General Medicine, medicine.disease, Spermatozoa, Sperm, Human genetics, Semen Analysis, Reproductive Medicine, Chromosomes, Human, Pair 8, Developmental Biology, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b0849e5c2080deb8412019693804f0
https://doi.org/10.1007/s10815-011-9621-x

المؤلفون: Meriem Mehdi, Hatem Elghezal, Ali Saad, Sonia Brahem

المصدر: Urology. 77:1343-1348

مصطلحات موضوعية: Adult, Male, Urology, Biotin, Aneuploidy, Semen, DNA Fragmentation, In situ hybridization, Chromosomes, Andrology, Pregnancy, In Situ Nick-End Labeling, medicine, Humans, In Situ Hybridization, Fluorescence, Infertility, Male, Globozoospermia, Chromosome Aberrations, Genetics, medicine.diagnostic_test, business.industry, Prognosis, medicine.disease, Sperm, Fertilization, DNA fragmentation, Female, business, Acrosome, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1c5ff04797616c9c0f725cf6c34cced
https://doi.org/10.1016/j.urology.2010.12.015