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A NEW HGPRT-DEFICIENT PHENOTYPE.

Other title
UN NOUVEAU PHENOTYPE DE DEFICIT EN HGPRT. (fr)
Author
KELLY S; HART EJ; DESJARDINS L
BIRTH DEFECTS INST., ALBANY, N.Y.
Source
J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 482-484; BIBL. 17REF.
Document type
Serial Issue
Language
English
Keyword (fr)
HYPERURICEMIE HEREDITAIRE ENCEPHALOPATHIE MALADIE HEREDITAIRE METABOLISME PROTEINE ENFANT DEFICIT HEREDITAIRE ENZYME HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE RETARD MENTAL CONVULSION FORME ATYPIQUE SIGNE METABOLISME TROUBLE HEREDITAIRE HOMME LESCH NYHAN SYNDROME OBSERVATION MALADIES METABOLIQUES GENETIQUE NEUROLOGIE
Keyword (en)
METABOLIC DISEASES GENETICS NEUROLOGY
Keyword (es)
ENFERMEDADES METABOLICAS GENETICA NEUROLOGIA
Classification
Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A31 Biotechnology / 002A31C Methods. Procedures. Technologies / 002A31C02 Genetic technics

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B21 Endocrinopathies

Discipline
Biotechnology Endocrinopathies Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL733623405

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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