Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26–q26.1 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1993-03

AUTHORS

Mohammad Faiyaz ul Haque, Siegfried Uhlhaas, Michael Knapp, Herdit Schüler, Waltraut Friedl, Mahmud Ahmad, Peter Propping

ABSTRACT

A large inbred kindred from Pakistan in which an isolated type of split-hand/split-foot anomaly is transmitted as an X-chromosomal trait has previously been described. An X/autosomal translocation and an X-chromosomal rearrangement have been excluded by cytogenetic studies. In order to map the gene responsible for this disorder, linkage analysis has been performed by using 14 highly polymorphic DNA markers distributed over the whole X chromosome. Two-point linkage analysis between the disease locus and X-chromosomal marker loci gives maximal lod scores at theta = 0.00 with the loci DXS294 (Zmax = 5.13) and HPRT (Zmax = 4.43), respectively, suggesting that the gene for the X-chromosomal split-hand/split-foot anomaly is localized at Xq26-q26.1. More... »

PAGES

17-19

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00230215

DOI

http://dx.doi.org/10.1007/bf00230215

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014342027

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8454282


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