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BEITRAG ZUM SIEMENS-I-SYNDROME

Other title
CONTRIBUTION AU SYNDROME DE SIEMENS. I (fr)
Author
KOEHLER U; MUELLER W; SCHUBERT H; LUKASSEK B
MED. AKAD. ERFURT, AUGENKLIN./ERFURT 5060/DDR
Source
KLIN. MONATSBL. AUGENHEILKD.; ISSN 0023-2165; DEU; DA. 1981; VOL. 179; NO 2; PP. 123-127; ABS. ENG; BIBL. 14 REF.
Document type
Article
Language
German
Keyword (fr)
ETUDE FAMILIALE KERATOPATHIE HOMOGREFFE CORNEE SYNDROME HEREDITAIRE KERATOSE PILAIRE ALOPECIE ENFANT PEAU PATHOLOGIE MALADIE HEREDITAIRE MALFORMATION OEIL PAUPIERE CHIRURGIE HOMME KERATOSIS FOLLICULAIRES SPINULOSA DECALVANS DERMATOLOGIE OPHTALMOLOGIE GENETIQUE
Keyword (en)
FAMILY STUDY KERATOPATHY CORNEA PILARIS KERATOSIS ALOPECIA CHILD GENETIC DISEASE MALFORMATION SURGERY MAN DERMATOLOGY OPHTALMOLOGY GENETICS
Keyword (es)
DERMATOLOGIA OFTALMOLOGIA GENETICA
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 / 002B08 Dermatology

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B09 Ophthalmology

Discipline
Biotechnology Dermatology Ophthalmology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL82X0006188

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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