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Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II

Author
NEUMANN, H. P. H1 ; ENG, C; MULLIGAN, L. M; GLAVAC, D; ZÄUNER, I1 ; PONDER, B. A. J; CROSSEY, P. A; MAHER, E. R; BRAUCH, H
[1] Albert-Ludwigs-univ. Freiburg, dep. nephrology hypertension, Germany
Source

JAMA, the journal of the American Medical Association. 1995, Vol 274, Num 14, pp 1149-1151 ; ref : 21 ref

ISSN
0098-7484
Scientific domain
General medicine general surgery
Publisher
American Medical Association, Chicago, IL
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Etude familiale Evaluation performance Exploration Homme Lignée germinale Mutation Polyadénomatose endocrinienne II Endocrinopathie Maladie héréditaire Tumeur maligne
Keyword (en)
Family study Performance evaluation Exploration Human Germ line Mutation Multiple endocrine neoplasia type II Endocrinopathy Genetic disease Malignant tumor
Keyword (es)
Estudio familiar Evaluación prestación Exploración Hombre Línea germinal Mutación Neoplasia endocrina múltiple tipo II Endocrinopatía Enfermedad hereditaria Tumor maligno
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B21 Endocrinopathies / 002B21G General aspects. Associated endocrine diseases. Endocrine paraneoplasic syndromes

Discipline
Endocrinopathies
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
2895779

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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