Literature DB >> 3410461

The coagulation factor VII regulator is located on 8p23.1.

K Fagan1, I Wilkinson, M Allen, S Brownlea.   

Abstract

Cytogenetic and coagulation studies have been performed on two patients with different abnormalities of chromosome 8, i.e. del(8p23.1----pter) and dup(8q23.1----qter). Results confirm the existence of a regulatory mechanism for clotting factor VII on chromosome 8 and define its location to the p23.1----p23.2 region.

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Year:  1988        PMID： 3410461     DOI： 10.1007/bf00282178

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  13 in total

1.  Coagulation studies in patients with trisomy 8 syndrome.

Authors:  S Stenbjerg; S Husted; A Bernsen; P Jacobsen; J Nielsen; K Rasmussen
Journal:  Ann Genet       Date:  1975-12

2.  [Coagulation factor VII deficiency in 3 patients with trisomy 8].

Authors:  J de Grouchy; F Josso; S Beguin; C Turleau; P Jalbert; C Laurent
Journal:  Ann Genet       Date:  1974-06

3.  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

4.  Factor VII antibody-neutralizing material in hereditary and acquired factor VII deficiency.

Authors:  S H Goodnight; D I Feinstein; B Osterud; S I Rapaport
Journal:  Blood       Date:  1971-07       Impact factor: 22.113

5.  Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.

Authors:  J de Grouchy; M D Dautzenberg; C Turleau; S Beguin; F Chavin-Colin
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  A simple and reliable method of chromosome banding for prenatal cytogenetics using a bromodeoxyuridine pulse.

Authors:  S Z Eichenbaum; E J Krumins
Journal:  Prenat Diagn       Date:  1983-10       Impact factor: 3.050

Review 7.  Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.

Authors:  W B Dobyns; G W Dewald; R O Carlson; D D Mair; V V Michels
Journal:  Am J Med Genet       Date:  1985-09

8.  The 8p- syndrome.

Authors:  J A Reiss; P M Brenes; J Chamberlin; R E Magenis; E W Lovrien
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

9.  Complete and partial trisomy of different segments of chromosome 8: case reports and review.

Authors:  R M Fineman; R C Ablow; W R Breg; S D Wing; J S Rose; S L Rothman; J Warpinski
Journal:  Clin Genet       Date:  1979-12       Impact factor: 4.438

10.  Monosomy 8p: an easily overlooked syndrome.

Authors:  A H Bröcker-Vriends; P D Mooij; F van Bel; G C Beverstock; J J van de Kamp
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318
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  4 in total

1.  Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome.

Authors:  S L Graw; T Sample; J Bleskan; E Sujansky; D Patterson
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

Review 2.  Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

Authors:  M J Pettenati; N Rao; C Johnson; R Hayworth; K Crandall; O Huff; I T Thomas
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

3.  Investigation of a common canine factor VII deficiency variant in dogs with unexplained bleeding on autopsy.

Authors:  Jessica A Clark; Stephen B Hooser; Dayna L Dreger; Grant N Burcham; Kari J Ekenstedt
Journal:  J Vet Diagn Invest       Date:  2022-08-10       Impact factor: 1.569

4.  Acute Myelogenous Leukemia With Trisomy 8 and Concomitant Acquired Factor VII Deficiency.

Authors:  Leila Moosavi; Jonathan Bowen; Jeffrey Coleman; Arash Heidari; Everardo Cobos
Journal:  J Investig Med High Impact Case Rep       Date:  2019 Jan-Dec
  4 in total

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