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Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.

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Title: Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
Authors: Hussen DF; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Kamel AK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Mekkawy MK; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Ashaat EA; Clinical Genetics Department, National Research Centre, Cairo, Egypt., El Ruby MO; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
Source: Molecular syndromology [Mol Syndromol] 2020 Dec; Vol. 11 (5-6), pp. 284-295. Date of Electronic Publication: 2020 Sep 23.
Publication Type: Journal Article
Journal Info: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
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  Data: <searchLink fieldCode="AU" term="%22Hussen+DF%22">Hussen DF</searchLink>; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22Kamel+AK%22">Kamel AK</searchLink>; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22Mekkawy+MK%22">Mekkawy MK</searchLink>; Human Cytogenetics Department, National Research Centre, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22Ashaat+EA%22">Ashaat EA</searchLink>; Clinical Genetics Department, National Research Centre, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22El+Ruby+MO%22">El Ruby MO</searchLink>; Clinical Genetics Department, National Research Centre, Cairo, Egypt.
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  Data: <searchLink fieldCode="JN" term="%22101525192%22">Molecular syndromology</searchLink> [Mol Syndromol] 2020 Dec; Vol. 11 (5-6), pp. 284-295. <i>Date of Electronic Publication: </i>2020 Sep 23.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22S%2E+Karger%22">S. Karger </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101525192 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>1661-8769 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216618769%22">16618769 </searchLink><i>NLM ISO Abbreviation: </i>Mol Syndromol <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1159/000510428
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      – Code: eng
        Text: English
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        StartPage: 284
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      – TitleFull: Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
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            NameFull: Hussen DF
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            NameFull: Kamel AK
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            NameFull: Mekkawy MK
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            NameFull: Ashaat EA
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            NameFull: El Ruby MO
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            – D: 01
              M: 12
              Text: 2020 Dec
              Type: published
              Y: 2020
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