Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization ; volume:7 ; number:1 ; day:25 ; month:9 ; year:2014 ; pages:1-6 ; date:12.2014
Molecular cytogenetics ; 7, Heft 1 (25.9.2014), 1-6, 12.2014
- Creator
-
Liu, Nian
Yan, Jiong
Chen, Xinlin
Song, Jieping
Wang, Bo
Yao, Yanyi
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13039-014-0062-y
- URN
-
urn:nbn:de:101:1-2021081409373269591237
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 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
- Liu, Nian
- Yan, Jiong
- Chen, Xinlin
- Song, Jieping
- Wang, Bo
- Yao, Yanyi
- SpringerLink (Online service)
Other Objects (12)
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome
Application of a target array Comparative Genomic Hybridization to prenatal diagnosis
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Hybridization.
Deletion of BSG1 in Chlamydomonas reinhardtii leads to abnormal starch granule size and morphology
Assessment of 1p/19q deletion by flourescence insitu hybridization (FISH) in glioma patients from Andhrapradesh
Diagnosis pitfall of interstitial pregnancy: a case report of a term pregnancy with abnormal placentation
Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype
Prenatal inflammation causes obesity and abnormal lipid metabolism via impaired energy expenditure in male offspring
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome
Application of a target array Comparative Genomic Hybridization to prenatal diagnosis
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Hybridization.
Deletion of BSG1 in Chlamydomonas reinhardtii leads to abnormal starch granule size and morphology
Assessment of 1p/19q deletion by flourescence insitu hybridization (FISH) in glioma patients from Andhrapradesh
Diagnosis pitfall of interstitial pregnancy: a case report of a term pregnancy with abnormal placentation
Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype
Prenatal inflammation causes obesity and abnormal lipid metabolism via impaired energy expenditure in male offspring
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome
Application of a target array Comparative Genomic Hybridization to prenatal diagnosis
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Hybridization.
Deletion of BSG1 in Chlamydomonas reinhardtii leads to abnormal starch granule size and morphology
Assessment of 1p/19q deletion by flourescence insitu hybridization (FISH) in glioma patients from Andhrapradesh
Diagnosis pitfall of interstitial pregnancy: a case report of a term pregnancy with abnormal placentation
Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype