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PRADER-WILLI SYNDROME: ARE THERE POPULATION DIFFERENCES.

Author
BUTLER MG; WEAVER DD; MEANEY FJ
INDIANA UNIV., SCHOOL MEDICINE/INDIANAPOLIS IN/USA
Source
CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 5; PP. 292-294; BIBL. 8 REF.
Document type
Article
Language
English
Keyword (fr)
PRADER LABHARD WILLI SYNDROME NEGROIDE CHROMOSOME D15 ANORMAL DELETION PARTIELLE ADOLESCENT FEMME CHIMERISME ABERRATION CHROMOSOMIQUE HYPOTONIE MUSCULAIRE ARRIERATION MENTALE RETARD STATURAL OBESITE HYPOGONADISME GENETIQUE HOMME
Keyword (en)
PRADER LABHARD WILLI SYNDROME NEGROID ABNORMAL D15 CHROMOSOME PARTIAL DELETION ADOLESCENT WOMAN CHIMERISM CHROMOSOMAL ABERRATION MUSCULAR HYPOTONIA MENTAL RETARDATION GROWTH RETARDATION OBESITY HYPOGONADISM GENETICS HUMAN
Keyword (es)
GENETICA
Classification
Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A31 Biotechnology / 002A31C Methods. Procedures. Technologies / 002A31C02 Genetic technics

Discipline
Biotechnology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL83X0315502

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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