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Article

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

BMC medical genetics - 6 Feb 2020

Hadj Amor Meriam, Dimassi Sarra, Taj Amel, Slimani Wafa, Hannachi Hanene, Mlika Adnene, Ben Helel Khaled, Saad Ali, Mougou-Zerelli Soumaya

Abstract excerpt

BACKGROUND: While Miller-Dieker syndrome critical region deletions are well known delineated anomalies, submicroscopic duplications in this region have recently emerged as a new distinctive syndrome. So far, only few cases have been described overlapping 17p13.3 duplications. METHODS: In this study, we report on clinical and cytogenetic characterization of two new cases involving 17p13.3 and 3p26 chromosomal...

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Identifiers

PMID: 32028920
DOI: 10.1186/s12881-020-0966-9
PMCID: PMC7006381

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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