Molka Kammoun - Department of Human Genetics, KU Leuven

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论文共 33 篇作者统计合作学者相似作者

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Clinical and Molecular Characterization of 1q43q44 Deletion and Corpus Callosum Malformations: 2 New Cases and Literature Review

Bochra Khadija,Khouloud Rjiba,Sarra Dimassi, Wafa Dahleb,Molka Kammoun, Hanen Hannechi,Najoua Miladi,Neziha Gouider-khouja,Ali Saad,Soumaya Mougou-Zerelli

Molecular Cytogeneticsno. 1 (2022): 1-12

引用1浏览0引用

Autism in Patients with Williams-Beuren Syndrome: A Re-Evaluation of 31 Tunisian Patients’ Phenotype

Soumaya Mougou-Zerelli, Rim Khelifi,Afef Jelloul,Houda Ajmi,Sarra Dimassi,Wafa Slimani, Najla Soyeh,Khouloud Rjiba, Manel Dardour,Hamza Hadj Abdallah, Hend Dridi,Asma Guedria,Molka Kammoun,Hela Ben Khelifa, Hayet Mkadem, Ines Hssairi Guidara, H. Ben Hamida,Khaled Ben Helel, Habib Kharrat, Essia Sboui, Elies Naffeti,N. Gaddour, Faouzi Maatouk,Hatem El Ghezal,Ali Saad, Ons Nouira, Afif Zouari

Research Square (Research Square) (2022)

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Further Report of MEDS Syndrome: Clinical and Molecular Delineation of a New Tunisian Case

Khouloud Rjiba,Najla Soyah,Molka Kammoun,Imen Hadj Hmida,Ali Saad,Kenneth Mcelreavey,Soumaya Mougou-Zerelli

European Journal of Medical Geneticsno. 9 (2021)

引用3浏览0WOS引用

Élargissement Du Spectre Phénotypique Du Syndrome Meds (microcéphalie, Épilepsie Et Diabète Néonatal) Lié Au Gène IER3IP1 : À Propos D’un Cas Tunisien Présentant Un Hypogonadisme

K. Rjiba,N. Soyah,M. Kammoun, I. Hadj Hmida,A. Saad,K. Mcelreavey,S. Mougou-Zerelli

Annales d'endocrinologie（2020）

引用0浏览0引用

Array CGH and FISH characterization of six new cases of Small Supernumerary Marker Chromosomes encompassing the 15q11q13 region

Wafa Slimani,Molka Kammoun, Ahlem Atig, Soussen Meddeb,Jihen Mathlouthi,Damien Sanlaville,Thomas Liehr,Ali Saad,Soumaya Mougou-Zerelli

MOLECULAR CYTOGENETICS（2019）

引用0浏览0引用

Pathogenic Variants in CDC45 on the Remaining Allele in Patients with a Chromosome 22q11.2 Deletion Result in a Novel Autosomal Recessive Condition

Marta Unolt,Molka Kammoun,Beata Nowakowska,Gail E. Graham,T. Blaine Crowley,Matthew S. Hestand,Wolfram Demaerel,Maciej Geremek,Beverly S. Emanuel,Elaine H. Zackai,Joris R. Vermeesch,Donna McDonald-McGinn

Genetics in Medicine（2019）

引用19浏览0WOS引用

Clinical and Molecular Findings in Nine New Cases of Tetrasomy 18p Syndrome: FISH and Array CGH Characterization

Wafa Slimani,Hela Ben Khelifa,Sarra Dimassi, Fatma-Zohra Chioukh,Afef Jelloul,Molka Kammoun,Hanene Hannachi,Sarra Bouslah, Nesrine Jammali,Damien Sanlaville,Ali Saad,Soumaya Mougou-Zerelli

MOLECULAR CYTOGENETICS (2019)

引用8浏览0WOS引用

Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing

Molka Kammoun,Erika Souche,Paul Brady,Jia Ding,Nele Cosemans,Eduard Gratacos,Koen Devriendt,Elisenda Eixarch,Jan Deprest,Joris Robert Vermeesch

PRENATAL DIAGNOSIS（2018）

引用28浏览0WOS引用

Pathogenic Variants in E3 Ubiquitin Ligase RLIM/RNF12 Lead to a Syndromic X-linked Intellectual Disability and Behavior Disorder

Molecular psychiatry（2018）

引用23浏览0WOSNATURE引用

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