Literature DB >> 14818695

Familial congenital labile factor deficiency with syndactylism; investigation on the mode of action of the labile factor.

A DE VRIES, Y MATOTH, Z SHAMIR.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS

Mesh:

Substances:

Year:  1951        PMID: 14818695     DOI: 10.1159/000203820

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


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  8 in total

1.  Idiopathic hyperlipemia. A case report in a nine-year-old Negro girl with an associated deficiency in labile factor and prothrombin.

Authors:  S HARA; G E ACKAOUY; E P CRUMP
Journal:  J Natl Med Assoc       Date:  1962-09       Impact factor: 1.798

2.  [Differential diagnosis of congenital Stuart factor deficiency].

Authors:  M H HORDER
Journal:  Klin Wochenschr       Date:  1959-04-15

3.  Biochemical genetics of blood coagulation.

Authors:  J B GRAHAM
Journal:  Am J Hum Genet       Date:  1956-06       Impact factor: 11.025

4.  The laboratory detection of heterozygotes.

Authors:  D Y HSIA
Journal:  Am J Hum Genet       Date:  1957-06       Impact factor: 11.025

5.  The measurement of prothrombin in plasma; a case of prothrombin deficiency.

Authors:  R BIGGS; A S DOUGLAS
Journal:  J Clin Pathol       Date:  1953-02       Impact factor: 3.411

6.  Hemorrhagic varicella in parahemophilia.

Authors:  A Girolami; R Scarpa; P Cadrobbi
Journal:  Blut       Date:  1972-11

Review 7.  Genetics of human blood coagulation.

Authors:  C B Kerr
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

8.  [Congenital factor V deficiency (Owren's disease)].

Authors:  F HENI; I KRAUSS
Journal:  Klin Wochenschr       Date:  1954-07-15
  8 in total

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