Literature DB >> 4170833

Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia.

J C Jacobs, A de Capoa, E McGilvray, J H Morse, J N Schullinger, W A Blanc, W C Heird, O J Miller, R D Rossen, R A Walzer.   

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Year:  1968        PMID： 4170833     DOI： 10.1016/s0140-6736(68)91467-0

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  7 in total

1.  [Cytogenetic, immunological and cytological family studies in Bloom's syndrome].

Authors:  J Keutel
Journal:  Humangenetik       Date:  1969-10

2.  Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.

Authors:  D Schuler; A Kiss; F Fábián
Journal:  Humangenetik       Date:  1969

3.  [Tendency for chromosome breaks in Russel's syndrome].

Authors:  E Ganner; A Schwingshackl
Journal:  Klin Wochenschr       Date:  1970-05-15

4.  Graft-versus-host disease following blood transfusions.

Authors:  H Pflieger
Journal:  Blut       Date:  1983-02

5.  Four families with immunodeficiency and chromosome abnormalities.

Authors:  D C Candy; A R Hayward; D T Hughes; L Layward; J F Soothill
Journal:  Arch Dis Child       Date:  1979-07       Impact factor: 3.791

6.  Leukocytic function in hypogammaglobulinemia.

Authors:  I D Mickenberg; R K Root; S M Wolff
Journal:  J Clin Invest       Date:  1970-08       Impact factor: 14.808

7.  Synthesis of the first component of human complement in vitro.

Authors:  H R Colten; J M Gordon; T Borsos; H J Rapp
Journal:  J Exp Med       Date:  1968-10-01       Impact factor: 14.307
  7 in total

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