A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5 ; volume:15 ; number:1 ; day:11 ; month:2 ; year:2014 ; pages:1-9 ; date:12.2014
BMC medical genetics ; 15, Heft 1 (11.2.2014), 1-9, 12.2014
- Creator
-
Krgovic, Danijela
- Contributor
-
Blatnik, Ana
Burmas, Ante
Zagorac, Andreja
Kokalj Vokac, Nadja
SpringerLink (Online service)
- DOI
-
10.1186/1471-2350-15-21
- URN
-
urn:nbn:de:1111-2016081217403
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:58 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
- Krgovic, Danijela
- Blatnik, Ana
- Burmas, Ante
- Zagorac, Andreja
- Kokalj Vokac, Nadja
- SpringerLink (Online service)
Other Objects (12)
Efficient error correction algorithms for gene tree reconciliation based on duplication, duplication and loss, and deep coalescence
Epilepsies in Children with 2q24.3 Deletion/Duplication
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability
First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p
Inferring Pareto-optimal reconciliations across multiple event costs under the duplication-loss-coalescence model
Efficient genome-scale phylogenetic analysis under the duplication-loss and deep coalescence cost models
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Efficient error correction algorithms for gene tree reconciliation based on duplication, duplication and loss, and deep coalescence
Epilepsies in Children with 2q24.3 Deletion/Duplication
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability
First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p
Inferring Pareto-optimal reconciliations across multiple event costs under the duplication-loss-coalescence model
Efficient genome-scale phylogenetic analysis under the duplication-loss and deep coalescence cost models
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Efficient error correction algorithms for gene tree reconciliation based on duplication, duplication and loss, and deep coalescence
Epilepsies in Children with 2q24.3 Deletion/Duplication
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability
First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p
Inferring Pareto-optimal reconciliations across multiple event costs under the duplication-loss-coalescence model
Efficient genome-scale phylogenetic analysis under the duplication-loss and deep coalescence cost models
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance