Article
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 Feb 2024
Elidrissi Errahhali Manal, Elidrissi Errahhali Mounia, Ramdani Sara, Lhousni Saida, Benajiba Noufissa, Rkain Maria, Babakhouya Abdeladim, Elouali Aziza, Ghanam Ayad, Amrani Rim, Messaoudi Sahar, Ayyad Anass, Oneib Bouchra, Mimouni Ahmed, Saadi Hanane, Allaoui Sanae, Ouarzane Meryem, Guichet Agnès, Charif Majida, Boulouiz Redouane, Bellaoui Mohammed
Abstract excerpt
BACKGROUND: Chromosomal abnormalities are the main cause of birth defects, intellectual disability, and miscarriages. They contribute to significant human morbidity and infant mortality. Here we report for the first time the chromosomal abnormalities encountered in the population of Eastern Morocco. Furthermore, we describe a new case of a de novo partial trisomy 13q combined with a terminal deletion in an...
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