Literature DB >> 6982968

Prenatal diagnosis of severe combined immunodeficiency.

A Durandy, Y Dumez, D Guy-Grand, C Oury, R Henrion, C Griscelli.   

Abstract

Entities:  

Mesh:

Year:  1982        PMID: 6982968     DOI: 10.1016/s0022-3476(82)80029-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  5 in total

1.  Prenatal exclusion of purine nucleoside phosphorylase deficiency.

Authors:  E Carapella De Luca; M Stegagno; C Dionisi Vici; R Paesano; L D Fairbanks; G S Morris; H A Simmonds
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

2.  Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

Authors:  G de Saint Basile; B Arveiler; I Oberlé; S Malcolm; R J Levinsky; Y L Lau; M Hofker; M Debre; A Fischer; C Griscelli
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

3.  Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiency.

Authors:  D C Linch; R J Levinsky; C H Rodeck; K A Maclennan; H A Simmonds
Journal:  Clin Exp Immunol       Date:  1984-05       Impact factor: 4.330

4.  Development of lymphocyte subpopulations identified by monoclonal antibodies in human fetuses.

Authors:  W A Kamps; M D Cooper
Journal:  J Clin Immunol       Date:  1984-01       Impact factor: 8.317

5.  Development of the immune system.

Authors:  A Durandy
Journal:  Infect Dis Obstet Gynecol       Date:  1997
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.