Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.

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Title: Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.
Authors: Khadija B; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.; Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia.; Common Service Units for Research in Genetics, Faculty of Medicine of Sousse, University of Sousse, Sousse, Tunisia., Rjiba K; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.; Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia.; Common Service Units for Research in Genetics, Faculty of Medicine of Sousse, University of Sousse, Sousse, Tunisia., Dimassi S; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.; Common Service Units for Research in Genetics, Faculty of Medicine of Sousse, University of Sousse, Sousse, Tunisia., Dahleb W; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.; Higher Institute of Biotechnology, Monastir University, Monastir, Tunisia., Kammoun M; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia., Hannechi H; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia., Miladi N; Medical Maghreb, El Manar 3, 2092, Tunis, Tunisia.; University of Tunis El Manar, 2092 El Manar 1, Tunis, Tunisia., Gouider-Khouja N; Head of Department at the National Institute of Neurology Tunis Head of RU On Movement Disorders, Tunis, Tunisia., Saad A; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.; Common Service Units for Research in Genetics, Faculty of Medicine of Sousse, University of Sousse, Sousse, Tunisia., Mougou-Zerelli S; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia. mougousoumaya@yahoo.fr.; Common Service Units for Research in Genetics, Faculty of Medicine of Sousse, University of Sousse, Sousse, Tunisia. mougousoumaya@yahoo.fr.
Source: Molecular cytogenetics [Mol Cytogenet] 2022 Oct 03; Vol. 15 (1), pp. 42. Date of Electronic Publication: 2022 Oct 03.
Publication Type: Journal Article
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101317942 Publication Model: Electronic Cited Medium: Print ISSN: 1755-8166 (Print) Linking ISSN: 17558166 NLM ISO Abbreviation: Mol Cytogenet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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ISSN:1755-8166
DOI:10.1186/s13039-022-00620-2