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Prenatal diagnosis of triosephosphate isomerase deficiency

Author
ARYA, R1 ; LALLOZ, M. R. A1 ; NICOLAIDES, K. H1 ; BELLINGHAM, A. J1 ; LAYTON, D. M1
[1] Department of Haematological Medicine and the Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, United Kingdom
Source

Blood. 1996, Vol 87, Num 11, pp 4507-4509 ; ref : 13 ref

ISSN
0006-4971
Scientific domain
Medical oncology; Hematology
Publisher
The Americain Society of Hematology, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Biologie moléculaire Diagnostic Déficit Foetus Glycolytic enzyme Gène Génotype Homme Maladie héréditaire Mutation Prénatal Séquence nucléotide Triose-phosphate isomerase Enzyme Intramolecular oxidoreductases Isomerases
Keyword (en)
Molecular biology Diagnosis Deficiency Fetus Glycolytic enzyme Gene Genotype Human Genetic disease Mutation Prenatal Nucleotide sequence Triose-phosphate isomerase Enzyme Intramolecular oxidoreductases Isomerases
Keyword (es)
Biología molecular Diagnóstico Déficiencia Feto Glycolytic enzyme Gen Genotipo Hombre Enfermedad hereditaria Mutación Prenatal Secuencia nucleótido Triose-phosphate isomerase Enzima Intramolecular oxidoreductases Isomerases
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D03 Carbohydrates (enzymatic deficiencies). Glycogenosis

Discipline
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3106269

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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