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Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.

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Title: Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
Authors: Komlósi, Katalin1,2, Duga, Balázs1,2, Hadzsiev, Kinga1,2, Czakó, Márta1,2, Kosztolányi, György1,2, Fogarasi, András3, Melegh, Béla1,2 melegh.bela@pte.hu
Source: Molecular Cytogenetics (17558166). 2015, Vol. 8 Issue 1, p1-6. 6p.
Database: Academic Search Ultimate
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  Data: Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
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PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=102041901
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s13039-015-0118-7
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        Text: English
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      – TitleFull: Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
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            NameFull: Komlósi, Katalin
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            NameFull: Duga, Balázs
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            NameFull: Hadzsiev, Kinga
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            NameFull: Czakó, Márta
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            NameFull: Kosztolányi, György
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            NameFull: Fogarasi, András
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            NameFull: Melegh, Béla
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              Text: 2015
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            – TitleFull: Molecular Cytogenetics (17558166)
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