Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report ; volume:15 ; number:1 ; day:25 ; month:11 ; year:2014 ; pages:1-7 ; date:12.2014
BMC medical genetics ; 15, Heft 1 (25.11.2014), 1-7, 12.2014
- Creator
-
Luo, Shiyu
- Contributor
-
Huang, Wen
Xia, Qiuping
Xia, Yan
Du, Qian
Wu, Lingqian
Duan, Ranhui
SpringerLink (Online service)
- DOI
-
10.1186/s12881-014-0125-2
- URN
-
urn:nbn:de:1111-2016081217444
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:50 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
- Luo, Shiyu
- Huang, Wen
- Xia, Qiuping
- Xia, Yan
- Du, Qian
- Wu, Lingqian
- Duan, Ranhui
- SpringerLink (Online service)
Other Objects (12)
Intranuclear inclusions in a fragile X mosaic male
Retinoblastoma and mosaic 13q deletion: a case report
Mosaїc
Treatment effects of stimulant medication in young boys with fragile X syndrome
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
Mosaic deletion patterns of the human antibody heavy chain gene locus shown by Bayesian haplotyping
Fragile
Fragile
Fragile
Fragile
Fragile
Fragile
Intranuclear inclusions in a fragile X mosaic male
Retinoblastoma and mosaic 13q deletion: a case report
Mosaїc
Treatment effects of stimulant medication in young boys with fragile X syndrome
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
Mosaic deletion patterns of the human antibody heavy chain gene locus shown by Bayesian haplotyping
Fragile
Fragile
Fragile
Fragile
Fragile
Fragile
Intranuclear inclusions in a fragile X mosaic male
Retinoblastoma and mosaic 13q deletion: a case report
Mosaїc
Treatment effects of stimulant medication in young boys with fragile X syndrome
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
Mosaic deletion patterns of the human antibody heavy chain gene locus shown by Bayesian haplotyping
Fragile
Fragile
Fragile
Fragile
Fragile