- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8794
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report ; volume:15 ; number:1 ; day:6 ; month:6 ; year:2022 ; pages:1-8 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (6.6.2022), 1-8, 12.2022
- Creator
-
Dai, Jincheng
Zeng, Jun
Tan, Hongxi
Cai, Xiangsheng
Wu, Benqing
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12920-022-01274-0
- URN
-
urn:nbn:de:101:1-2022080322290095333358
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Dai, Jincheng
- Zeng, Jun
- Tan, Hongxi
- Cai, Xiangsheng
- Wu, Benqing
- SpringerLink (Online service)
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Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
Case report: early aortic valve degeneration associated with interstitial deletion of chromosome 2–46,XX,del (2)(q31.3; q32.2)
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Klinefelter syndrome with long-arm X-chromosome deletion
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Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
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Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
Case report: early aortic valve degeneration associated with interstitial deletion of chromosome 2–46,XX,del (2)(q31.3; q32.2)
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Klinefelter syndrome with long-arm X-chromosome deletion
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
Chromosome 3q29 deletion with gastrointestinal malformation: a case report
A deletion map of the WAGR region on chromosome II
Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
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