Literature DB >> 6745952

Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34).

R Ott, R A Pfeiffer.   

Abstract

In 7 patients with various anomalies of chromosome 13 coagulation, studies were performed. A 50% decrease of activities of factor VII and X were noted only in cases with deletion of 13 (q34) which supports the hypothesis that they are linked to this region.

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Year:  1984        PMID： 6745952     DOI： 10.1159/000153447

Source DB:  PubMed          Journal:  Hum Hered        ISSN： 0001-5652            Impact factor:   0.444


  4 in total

1.  Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9.

Authors:  M Rocchi; L Roncuzzi; R Santamaria; N Archidiacono; L Dente; G Romeo
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

2.  Clotting factors VII and X as useful markers of terminal deletion of chromosome 13.

Authors:  R A Pfeiffer; R Ott; K D Taben
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Exclusion of human chromosome 13q34 as the site of the cystic fibrosis mutation.

Authors:  P J Scambler; B J Wainwright; R T MacGillivray; M R Fung; R Williamson
Journal:  Am J Hum Genet       Date:  1986-04       Impact factor: 11.025

4.  Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.

Authors:  Barbara Preisler; Behnaz Pezeshkpoor; Atanas Banchev; Ronald Fischer; Barbara Zieger; Ute Scholz; Heiko Rühl; Bettina Kemkes-Matthes; Ursula Schmitt; Antje Redlich; Sule Unal; Hans-Jürgen Laws; Martin Olivieri; Johannes Oldenburg; Anna Pavlova
Journal:  J Clin Med       Date:  2021-01-18       Impact factor: 4.241
  4 in total

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