45,X mosaicism in a population-based biobank: implications for Turner syndrome
Genet Med
.
2019 Aug;21(8):1882-1883.
doi: 10.1038/s41436-018-0411-z.
Epub 2018 Dec 21.
Authors
Siddharth K Prakash
1
,
Melissa L Crenshaw
2
,
Philippe F Backeljauw
3
4
,
Michael Silberbach
5
,
Cindy Scurlock
6
,
Denise D Culin
7
,
Kelly C Ranallo
7
,
Angela E Lin
8
Affiliations
1
Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA.
[email protected]
.
2
Division of Genetics, Johns Hopkins All Children's Hospital, St Petersburg, FL, USA.
3
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
4
Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
5
Division of Pediatric Cardiology, Oregon Health & Science University, Portland, OR, USA.
6
Turner Syndrome Society of the United States, Houston, TX, USA.
7
Turner Syndrome Global Alliance, Overland Park, KS, USA.
8
Medical Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, MA, USA.
PMID:
30573796
DOI:
10.1038/s41436-018-0411-z
No abstract available
Publication types
Letter
Comment
MeSH terms
Adult
Biological Specimen Banks*
Chromosomes, Human, X
Humans
Mosaicism
Penetrance
Turner Syndrome*