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Expression of the gene defect in X-linked agammaglobulinemia

Author
CONLEY, M. E1 ; PICKARD, A. R; BUCKLEY, R. H; MILLER, D. S; FRASKIND, W. H; SINGER, J. W; FIALKOW, P. J
[1] Children's hosp., Philadelphia PA 19104, United States
Source

The New England journal of medicine. 1986, Vol 315, Num 9, pp 564-567 ; ref : 22 ref

CODEN
NEJMAG
ISSN
0028-4793
Scientific domain
General medicine general surgery
Publisher
Massachusetts Medical Society, Boston, MA
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Caractère lié au sexe Culture cellulaire Déficit Dépistage Etude familiale Expression génique Glucose-6-phosphate dehydrogenase Homme Hétérozygotie Immunodéficit héréditaire Bruton Immunopathologie Lymphocyte B Lymphocyte T
Keyword (en)
Sex linked character Cell culture Deficiency Screening Family study Gene expression Glucose«-6-»phosphate dehydrogenase Human Heterozygozity Infantile sex linked agammaglobulinemia Immunopathology B-Lymphocyte «T»-Lymphocyte
Keyword (es)
Caracter ligado al sexo Cultivo celular Deficit Deteccion Estudio familiar Expresion genetica Glucosa-6-fosfato deshidrogenasa Hombre Heterozigosis Inmunodeficiencia hereditaria Bruton Inmunopatologia Linfocito B Linfocito T
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B06 Immunopathology / 002B06D Immunodeficiencies. Immunoglobulinopathies / 002B06D01 Immunodeficiencies

Discipline
Immunopathology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
8145228

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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