Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review
- 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
-
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review ; volume:18 ; number:1 ; day:1 ; month:12 ; year:2017 ; pages:1-6 ; date:12.2017
BMC medical genetics ; 18, Heft 1 (1.12.2017), 1-6, 12.2017
- Urheber
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Tan, Li
- Beteiligte Personen und Organisationen
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Bi, Bo
Zhao, Peiwei
Cai, Xiaonan
Wan, Chunhui
Shao, Jianbo
He, Xuelian
SpringerLink (Online service)
- DOI
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10.1186/s12881-017-0501-9
- URN
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urn:nbn:de:101:1-2018082512083723616478
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:34 MESZ
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Beteiligte
- Tan, Li
- Bi, Bo
- Zhao, Peiwei
- Cai, Xiaonan
- Wan, Chunhui
- Shao, Jianbo
- He, Xuelian
- SpringerLink (Online service)
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