Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies ; volume:13 ; number:1 ; day:6 ; month:5 ; year:2020 ; pages:1-6 ; date:12.2020
Molecular cytogenetics ; 13, Heft 1 (6.5.2020), 1-6, 12.2020
- Urheber
-
Tan, Ya-Qi
Tan, Yue-Qiu
Cheng, De-Hua
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13039-020-00487-1
- URN
-
urn:nbn:de:101:1-2020071322463570384347
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:58 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Tan, Ya-Qi
- Tan, Yue-Qiu
- Cheng, De-Hua
- SpringerLink (Online service)
Ähnliche Objekte (12)
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report
Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations
SyRI: finding genomic rearrangements and local sequence differences from whole-genome assemblies
Apparently superluminal superfluids
Gene rearrangements in hormone receptor negative breast cancers revealed by mate pair sequencing
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
The influence of balanced complex chromosomal rearrangements on preimplantation embryonic development potential and molecular karyotype
Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review
Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing
TREATMENT OF THE APPARENTLY DROWNED
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report
Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations
SyRI: finding genomic rearrangements and local sequence differences from whole-genome assemblies
Apparently superluminal superfluids
Gene rearrangements in hormone receptor negative breast cancers revealed by mate pair sequencing
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
The influence of balanced complex chromosomal rearrangements on preimplantation embryonic development potential and molecular karyotype
Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review
Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing
TREATMENT OF THE APPARENTLY DROWNED
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report
Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations
SyRI: finding genomic rearrangements and local sequence differences from whole-genome assemblies
Apparently superluminal superfluids
Gene rearrangements in hormone receptor negative breast cancers revealed by mate pair sequencing
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
The influence of balanced complex chromosomal rearrangements on preimplantation embryonic development potential and molecular karyotype
Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature review
Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing