Mosaicism in Turner's syndrome
David Skuse and
Patricia Jacobs
Additional contact information
David Skuse: Institute of Child Health, University College London Medical School
Patricia Jacobs: Institute of Child Health, University College London Medical School
Nature, 1997, vol. 390, issue 6660, 569-569
Abstract:
Abstract Skuse and Jacobs reply — Henn and Zang argue that it is the presence of Y-chromosome sequences (presumably acting independently of sex steroids), rather than an imprinted gene on the X, that accounts both for male vulnerability to neurodevelopmental disorders of social cognition1 and for the poorer social adjustment of girls who have Turner's syndrome, with 45,Xm rather than 45,Xp. Unfortunately, without direct observations on the chromosome constitution of brain cells, Henn and Zang's hypothesis is not testable.
Date: 1997
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/37516 Abstract (text/html)
Access to the full text of the articles in this series is restricted.
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:390:y:1997:i:6660:d:10.1038_37516
Ordering information: This journal article can be ordered from
https://www.nature.com/
DOI: 10.1038/37516
Access Statistics for this article
Nature is currently edited by Magdalena Skipper
More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().