A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature von Ouboukss, Fatima, El Amrani, Zhour, Bouchahta, Hicham, Ratbi, Ilham, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz, Natiq, Abdelhafid

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The Genetic Facets of Dravet Syndrome: Recent Insights von Mouhi, Hinde El, Abbassi, Meriame, Jalte, Meryem, Natiq, Abdelhafid, Bouguenouch, Laila, Chaouki, Sana

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Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moro... von El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana

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Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma von Hamdaoui, Hasna, Natiq, Abdelhafid, Benlarroubia, Oumaima, Liehr, Thomas, Dehbi, Hind, Loukhmas, Latifa, Chegdani, Fatima

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Clinical characterization of 72 patients with del from different ethnic backgrounds von Méndez-Rosado, Luis A, de León-Ojeda, Norma, García, Alina, Sheth, Frenny, Gaadi, Asmaa, Bousfiha, Ahmed Aziz, Lehlimi, Mouna

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11p13 Deletion Syndrome: First Case in Morocco Detected by FISH von Natiq, Abdelhafid

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Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report von El Amrani, Zhour, Natiq, Abdelhafid, Sbiti, Aziza, Ratbi, Ilham, Liehr, Thomas, Sefiani, Abdelaziz, Sahli, Maryem

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Genome and Epigenome Disorders and Male Infertility: Feedback from 15 Years of Clinical and Research Experience von Montjean, Debbie, Beaumont, Marion, Natiq, Abdelhafid, Louanjli, Noureddine, Hazout, Andre, Miron, Pierre, Liehr, Thomas, Cabry, Rosalie, Ratbi, Ilham, Benkhalifa, Moncef

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Maternally Derived Complex Small Supernumerary Marker Chromosome 22 Associated with Cat-Eye Syndrome Like Features von Bouchahta, Hicham, Amrani, Zhour EL, Elalaoui, Siham Chafai, Ouboukss, Fatima, Sbiti, Aziza, Sbabou, Laila, Liehr, Thomas, Sefiani, Abdelaziz, Natiq, Abdelhafid

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Unique Female Patient with de novo 6q22.31q27 Duplication and Xq28 Deletion: Case Report and Brief Literature Review von Afif, Lamiae, El Amrani, Zhour, Sbiti, Aziza, Ratbi, Ilham, Jaouad, Imane Cherkaoui, El Kadiri, Youssef, Liehr, Thomas, Sefiani, Abdelaziz, Natiq, Abdelhafid

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Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness von Amasdl, Saadia, Smaili, Wiam, Natiq, Abdelhafid, Hassani, Amale, Sbiti, Aziza, Agadr, Aomar, Sanlaville, Damien, Sefiani, Abdelaziz

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Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis von Baala, Lekbir, Briault, Sylvain, Etchevers, Heather C, Laumonnier, Frédéric, Natiq, Abdelhafid, Amiel, Jeanne, Boddaert, Nathalie, Picard, Capucine, Sbiti, Aziza, Asermouh, Abdellah, Attié-Bitach, Tania, Encha-Razavi, Féréchté, Munnich, Arnold, Sefiani, Abdelaziz, Lyonnet, Stanislas

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Increased Clinical Pregnancy Outcomes; of Vitrified Blastocyst on Different Days of Embryo Development: Day 5 Compared to Day 6 Transfer von Zakaria, Mustafa, Steven, Marcuse F., Louanjli, Noureddine, Senhaji, Wassym R., Natiq, Abdelhafid, Zarqaoui, Mohammed

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Le diagnostic anténatal de la trisomie 21 par l'hybridation in situ en fluorescence (FISH): à propos des premiers tests réalisés au Maroc von Afaf Lamzouri, Abdelhafid Natiq, Mariam Tajir1, Mohamed Sendid, Abdelaziz Sefiani

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Impact of Serum Progesterone Value on Embryo Transfer Timing, and Pregnancy Rate von Zakaria, Mustafa, Louanjli, Noureddine, Al-ibraheemi, Aya, Ennaji, Mohamed, Senhaji, Wassym R., Natiq, Abdelhafid, Boutiche, Romaissa, Mbaye, Modou M., Zarqaoui, Mohamed

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Constitutional Partial Proximal Trisomy 14q11.2 to 14q21: Two New Moroccan Cases and Review of the Literature von Merhni, Hanane, Zerkaoui, Maria, Natiq, Abdelhafid, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz

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Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report von Amasdl, Saadia, Natiq, Abdelhafid, Elalaoui, Siham Chafai, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz

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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion von Natiq, Abdelhafid, Lysy, Philippe A., Gillemans, Nynke, Schaap, Rianne, Sefiani, Abdelaziz, Amzazi, Saaid, Chafai El‐Alaoui, Siham, Cantú, Ileana, Banjanin, Bella, van Lom, Kirsten, Harteveld, Cornelis L., Philipsen, Sjaak

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20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature von Amasdl, Saadia, Natiq, Abdelhafid, Sbiti, Aziza, Zerkaoui, Maria, Lyahyai, Jaber, Amzazi, Saaid, Liehr, Thomas, Sefiani, Abdelaziz

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Variation of exon 11 of the BRCA1 gene in patients with familial breast cancer at Mohammed VI center for treatment of cancers von Ibrahim Khalil, Ahmadaye, Bendahhou, Karima, Rhouda, Taha, Lyahyai, Jaber, Qachach, Fadwa, Zrhidri, AbdelAli, Natiq, Abdelhafid, Benider, Abdellatif, Mestaghanmi, Houriya

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