Literature DB >> 1083193

Coagulation studies in patients with trisomy 8 syndrome.

S Stenbjerg, S Husted, A Bernsen, P Jacobsen, J Nielsen, K Rasmussen.   

Abstract

Coagulation studies were performed in three patients with trisomy for chromosome No. 8. In contrast to the findings reported by others, all patients were found to have a normal coagulation status without sign of factor VII deficiency.

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Year:  1975        PMID： 1083193

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  5 in total

Review 1.  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

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

Authors:  K Fagan; I Wilkinson; M Allen; S Brownlea
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

3.  Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat.

Authors:  G I Lazjuk; I W Lurie; Y I Usova; D B Gurevich; M K Nedzved
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

4.  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

5.  Mosaicism for an additional partial chromosome 8: 46,XX/47,XX+der(8)(p21 leads to qter).

Authors:  R A Pfeiffer; E Kessel; E Rathgen; M Kulenkampff; T Nehring
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132
  5 in total

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