Karyotyping in the era of Genome Sequencing von Elghezal, Hatem

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Semen Parameters and Sperm DNA Fragmentation as Causes of Recurrent Pregnancy Loss von Brahem, Sonia, Mehdi, Meriem, Landolsi, Hanène, Mougou, Soumaya, Elghezal, Hatem, Saad, Ali

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Assessment of chromosomal aberrations, micronuclei and proliferation rate index in peripheral lymphocytes from Tunisian nurses handling cytotoxic drugs von Bouraoui, Sana, Brahem, Aicha, Tabka, Faten, Mrizek, Najib, Saad, Ali, Elghezal, Hatem

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Cytogenetic Profile and FLT3 Gene Mutations of Childhood Acute Lymphoblastic Leukemia von Alkhayat, Nawaf, Elborai, Yasser, Al Sharif, Omer, Al Shahrani, Mohammad, Alsuhaibani, Omar, Awad, Mohammed, Elghezal, Hatem, ben-abdallah Bouhajar, Inesse, Alfaraj, Mona, Al Mussaed, Eman, Alabbas, Fahad, Elyamany, Ghaleb

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Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome von AlKalaf, Heeba Y, AlHashem, Amal M, AlSaleh, Norah S, AlJohar, Norah M, Abo Thneen, Aliyah M, ElGhezal, Hatem M, Bouhjar, Inesse B, Tlili-Graiess, Kalthoum, Sahari, Atif H, Tabarki, Brahim M

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Rare cytogenetic abnormalities and their clinical relevance in pediatric acute leukemia of Saudi Arabian population von Alkhayat, Nawaf, Elyamany, Ghaleb, Elborai, Yasser, Sedick, Qanita, Alshahrani, Mohammad, Al Sharif, Omar, Alenezy, Abdulmalik, Hammdan, Amjad, Elghezal, Hatem, Alsuhaibani, Omar, Aljabry, Mansour S, AlMoshary, May, Al Mussaed, Eman

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Prevalence of chromosomal abnormalities in couples with recurrent miscarriage von Elghezal, Hatem, M.D, Hidar, Samir, M.D, Mougou, Soumaya, M.D, Khairi, Hedi, M.D, Saâd, Ali, M.D., Ph.D

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A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers von Bouraoui, Sana, Mougou, Soumaya, Drira, Afef, Tabka, Faten, Bouali, Nouha, Mrizek, Najib, Elghezal, Hatem, Saad, Ali

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A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure von Lakhal, Besma, Laissue, Paul, Braham, Rim, Elghezal, Hatem, Saâd, Ali, Fellous, Marc, Veitia, Reiner A.

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Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype von Ojeda, Diego, M.Sc, Lakhal, Besma, Ph.D, Fonseca, Dora Janneth, M.Sc, Braham, Rim, M.D, Landolsi, Hanène, Ph.D, Mateus, Heidi Eliana, M.D, Restrepo, Carlos Martín, M.D., Ph.D, Elghezal, Hatem, M.D, Saâd, Ali, M.D., Ph.D, Laissue, Paul, M.D., Ph.D

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Array‐CGH study of partial trisomy 9p without mental retardation von Abdallah Bouhjar, Inesse Ben, Hannachi, Hanane, Mougou Zerelli, Soumaya, Labalme, Audrey, Gmidène, Abir, Soyah, Najla, Missaoui, Sonia, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali

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De Novo CD5 Negative Blastic Mantle Cell Lymphoma Presented with Massive Bone Marrow Necrosis without Adenopathy or Organomegaly von Alotaibi, Sultan, Aljasem, Hassan, Al Mussaed, Eman, Alzahrani, Ali Matar, Elyamany, Ghaleb, Elghezal, Hatem

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The effects of male aging on semen quality, sperm DNA fragmentation and chromosomal abnormalities in an infertile population von Brahem, Sonia, Mehdi, Meriem, Elghezal, Hatem, Saad, Ali

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Chromosomal Microarray Analysis in a Girl With Mental Retardation and Spina Bifida von Ben Abdallah, Inesse, MS, Hannachi, Hanene, MS, Soyah, Najla, MD, Saad, Ali, MD, PhD, Elghezal, Hatem, MD, PhD

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De Novo Ring Chromosome 15: Molecular Cytogenetic and Clinical Characterization of First Case from Saudi Arabia von Alhashem, Amal, Alazmeh, Saria, Barakat, Ayla, Alfares, Ahmed, Elghezal, Hatem

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Analysis of Sperm Aneuploidies and DNA Fragmentation in Patients With Globozoospermia or With Abnormal Acrosomes von Brahem, Sonia, Mehdi, Meriem, Elghezal, Hatem, Saad, Ali

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Hypospadias in ring X syndrome von Elghezal, Hatem, Alfayez, Khowla, Ben Abdallah, Inesse, Alfares, Ahmed, Almazyad, Ayesh, Al Jasser, Abdullah, Almobadel, Nasser, Alsuhaibani, Omar, Alhashem, Amal

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Association of IMMP2L deletion with neurodevelopmental disorders: new case report and review of the literature von Bouhjar, Ines, Tabarki, Ibrahim, Alonazi, Hamoud, Alsulami, Mishal, Alhashem, Amal, Elghezal, Hatem

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Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation von Ben Khelifa, Hela, Soyah, Najla, Ben-Abdallah-Bouhjar, Inesse, Gritly, Ryma, Sanlaville, Damien, Elghezal, Hatem, Saad, Ali, Mougou-Zerelli, Soumaya

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Detection of DNA fragmentation and meiotic segregation in human with isolated teratozoospermia von Brahem, Sonia, Mehdi, Meriem, Elghezal, Hatem, Saad, Ali

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