Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1988-11

AUTHORS

A. Sefiani, D. Sinnett, L. Abel, S. Szpiro-Tapia, S. Heuertz, I. Craig, N. Fraser, T. A. Kruse, M. Frydman, M. O. Peter, J. L. Schmutz, S. Gilgenkrantz, G. Mitchell, J. Frézal, S. Melançon, L. Lavergne, D. Labuda, M. C. Hors-Cayla

ABSTRACT

Linkage studies have been performed in 5 incontinentia pigmenti (IP) families totaling 29 potentially informative meioses. Ten probes of the Xp arm were used, six of them were precisely localized on the X chromosome, using hamster X human somatic cell hybrids containing a broken X chromosome derived from an incontinentia pigmenti patient carrying an X;9 translocation [46,XX,t(X;9)(p11.21;q34)]. The following order for probes is proposed: pter - (DXS7, DXS146, DXS255) - IP1 - (DXS14, DXS90) - DXS106 - qter. The negative lod scores obtained exclude the possibility that in the families studied, the gene for IP is located in Xp11 or in the major part of the Xp arm. More... »

PAGES

282-286

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01790098

DOI

http://dx.doi.org/10.1007/bf01790098

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1033236293

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/3192215


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