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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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  Data: Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.
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  Data: <searchLink fieldCode="AU" term="%22Khadija+B%22">Khadija B</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Rjiba+K%22">Rjiba K</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Dimassi+S%22">Dimassi S</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Dahleb+W%22">Dahleb W</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Kammoun+M%22">Kammoun M</searchLink>; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.<br /><searchLink fieldCode="AU" term="%22Hannechi+H%22">Hannechi H</searchLink>; Laboratory of Human Cytogenetics, Department of Human Cytogenetics, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital, Sousse, Tunisia.<br /><searchLink fieldCode="AU" term="%22Miladi+N%22">Miladi N</searchLink>; Medical Maghreb, El Manar 3, 2092, Tunis, Tunisia.; University of Tunis El Manar, 2092 El Manar 1, Tunis, Tunisia.<br /><searchLink fieldCode="AU" term="%22Gouider-Khouja+N%22">Gouider-Khouja N</searchLink>; Head of Department at the National Institute of Neurology Tunis Head of RU On Movement Disorders, Tunis, Tunisia.<br /><searchLink fieldCode="AU" term="%22Saad+A%22">Saad A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Mougou-Zerelli+S%22">Mougou-Zerelli S</searchLink>; 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.
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  Data: <searchLink fieldCode="JN" term="%22101317942%22">Molecular cytogenetics</searchLink> [Mol Cytogenet] 2022 Oct 03; Vol. 15 (1), pp. 42. <i>Date of Electronic Publication: </i>2022 Oct 03.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101317942 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>1755-8166 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217558166%22">17558166 </searchLink><i>NLM ISO Abbreviation: </i>Mol Cytogenet <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1186/s13039-022-00620-2
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              Text: 2022 Oct 03
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