Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly ; volume:12 ; number:1 ; day:20 ; month:5 ; year:2011 ; pages:1-8 ; date:12.2011
BMC medical genetics ; 12, Heft 1 (20.5.2011), 1-8, 12.2011
- Urheber
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Liao, Hsiao-Mei
- Beteiligte Personen und Organisationen
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Fang, Jye-Siung
Chen, Yann-Jang
Wu, Kuang-Lun
Lee, Kuei-Fang
Chen, Chia-Hsiang
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-12-70
- URN
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urn:nbn:de:1111-2016071513405
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:51 MESZ
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Beteiligte
- Liao, Hsiao-Mei
- Fang, Jye-Siung
- Chen, Yann-Jang
- Wu, Kuang-Lun
- Lee, Kuei-Fang
- Chen, Chia-Hsiang
- SpringerLink (Online service)
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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- the new lacunae: a case report
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