Zobrazeno 1 - 10
of 33
pro vyhledávání: '"A. Kdissa"'
Autor:
G. Saad, A. Kdissa, A. Haj Khelil, M. Ajina, S. Hidar, S. Mougou, S. Ibala, K. Ach, M. Gribaa, A. Saad
Publikováno v:
Middle East Fertility Society Journal, Vol 23, Iss 4, Pp 268-272 (2018)
Introduction: In the present work, we aim to determine the frequency of Y microdeletions and to study the clinical and biological characteristics in idiopathic azoospermic and oligozoospermic men originating from the center of Tunisia. Methods: A sam
Externí odkaz:
https://doaj.org/article/f1ff681fd2454333b4630693fdb93e60
Autor:
Kdissa, Ameni, Brusgaard, Klaus, Ksiaa, Mahdi, Golli, Lamia, Hallara, Olfa, Ousager, Lilian Bomme, Manoubi, Wiem, Seghaier, Rihab Ben, Adala, Labiba, Halleb, Yosra, Saad, Ali, Hmila, Fahmi, Gribaa, Moez
Publikováno v:
In Cancer Genetics January 2020 240:45-53
Akademický článek
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Autor:
Saad, G., Kdissa, A., Haj Khelil, A., Ajina, M., Hidar, S., Mougou, S., Ibala, S., Ach, K., Gribaa, M., Saad, A.
Publikováno v:
In Middle East Fertility Society Journal December 2018 23(4):268-272
Autor:
Olfa Hallara, Labiba Adala, Ali Saad, Lamia Golli, Klaus Brusgaard, Wiem Manoubi, Mahdi Ksiaa, Moez Gribaa, Fahmi Hmila, Lilian Bomme Ousager, Rihab Ben Seghaier, Yosra Halleb, Ameni Kdissa
Publikováno v:
Kdissa, A, Brusgaard, K, Ksiaa, M, Golli, L, Hallara, O, Ousager, L B, Manoubi, W, Seghaier, R B, Adala, L, Halleb, Y, Saad, A, Hmila, F & Gribaa, M 2020, ' c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis ', Cancer genetics and cytogenetics, vol. 240, pp. 45-53 . https://doi.org/10.1016/j.cancergen.2019.10.007
INTRODUCTION: Familial adenomatous polyposis (FAP) is an autosomal dominant-inherited disease caused by germline variants in the APC gene. It is characterized by the development of hundreds to thousands of adenomatous polyps in colon and rectum. Rece
Akademický článek
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Autor:
Koussay El Euch, Bellakhdar Mouna, Amal Kdissa, Abdelkefi Mohamed, Meherzi Abir, Kermani Wassim, Ghammam Monia, Asma Ben Abdelkrim
Publikováno v:
Endocrine Abstracts.
Autor:
Nicole Fleischer, Grace M. Anbouba, Vandana Shashi, Thomas Meitinger, Damara Ortiz, Sumedha Ghate, Caleb Bupp, Maria J. Guillen Sacoto, Tiana M. Scott, Juliane Winkelmann, Felix Distelmaier, Sarah R Green, Dirk Klee, Carolyn R Serbinski, Lea Velsher, Michael T. Zimmermann, Meriel McEntagart, Gretchen Parsons, Patrick Yap, Evan H. Baugh, David S. Wargowski, Juan C Del Rey Jimenez, Anne K Olsen, Amy Armstrong-Javors, Victoria Mok Siu, Andrew Green, Nikita R. Dsouza, Elisabeth Graf, Sumit Punj, Matias Wagner, Anna Cereda, Naomi Meeks, Barbro Stadheim, Kirsty McWalter, Ingrid M. Wentzensen, Bert Callewaert, Rhonda E. Schnur, Emily Lancaster, Laurie A. Demmer, G. Bradley Schaefer, Kristin Lindstrom, Maria Iascone, Gonzalo Alonso Ramos-Rivera, Loren D M Pena, Amber Begtrup, Richard E. Person, Harrison Moore, Ameni Kdissa, Eric W. Klee, Dana Mittag, Jana Švantnerová, Ingrid Bader, Theresa Brunet, Johannes A. Mayr, Michael Zech, Jennifer A. Sullivan, Margot A. Cousin, Katharina Mayerhanser, Dagmar Wieczorek, Ralitza H. Gavrilova, Daryl A. Scott
Publikováno v:
GENETICS IN MEDICINE
Genetics in Medicine
Paediatrics Publications
Genet. Med. 23, 384–395 (2021)
Genetics in Medicine
Paediatrics Publications
Genet. Med. 23, 384–395 (2021)
PURPOSE: We sought to delineate the genotypic and phenotypic spectrum of female and male individuals with X-linked, MSL3-related disorder (Basilicata-Akhtar syndrome). METHODS: Twenty-five individuals (15 males, 10 females) with causative variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa02e378c99c12e2a54e9952d004b3ea
https://biblio.ugent.be/publication/8687772/file/8692632
https://biblio.ugent.be/publication/8687772/file/8692632
Publikováno v:
Endocrine Abstracts.
Autor:
Abdelkefi Mohamed, Monia Ghamam, Amal Kdissa, Mouna Khalifa, Mouna Bellakhdhar, Meherzi Abir, Kermani Wassim
Publikováno v:
Endocrine Abstracts.