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Megalocornea, macrocephaly, mental and motor retardation (MMMM)

Author
FRYDMAN, M; BERKENSTADT, M; RAAS-ROTHSCHILD, A; GOODMAN, R. M
Golda medical cent. Petah Tiqwa, Hasharon hosp., dep. pediatrics, Petah Tiqwa 49372, Israel
Source

Clinical genetics. 1990, Vol 38, Num 2, pp 149-154 ; ref : 14 ref

CODEN
CLGNAY
ISSN
0009-9163
Scientific domain
Genetics
Publisher
Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Enfant Etude cas Exploration clinique Macrocéphalie Mégalocornée Retard psychomoteur Homme Syndrome complexe
Keyword (en)
Child Case study Clinical investigation Macrocephaly Megalocornea Psychomotor retardation Human Complex syndrome
Keyword (es)
Niño Estudio caso Exploración clínica Macrocefalía Megalocórnea Retardo psicomotor Hombre Síndrome complejo
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics

Discipline
Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4616915

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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