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New case of contiguous gene syndrome at chromosome 8p11.2p12

Author
CAU, M1 ; CONGIU, R1 ; ORIGA, R1 ; GALANELLO, R1 ; MELIS, M. A1 ; NUCARO, A. L2
[1] Dipartimento di Scienze Biomediche e Biotecnologie Università di Cagliari, Cagliari, Italy
[2] Istituto di Neurogenetica e Neurofarmacologia CNR, Selargius, Cagliari, Italy
Source

American journal of medical genetics. = Neuropsychiatric genetics. 2005, Vol 136A, Num 2, pp 221-222, 2 p ; ref : 13 ref

CODEN
AJMGDA
ISSN
0148-7299
Scientific domain
Genetics
Publisher
Wiley-Liss, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Carte génétique Chromosome Etude cas Gène contigu syndrome Génétique Homme
Keyword (en)
Genetic mapping Chromosome Case study Contiguous gene syndrome Genetics Human
Keyword (es)
Mapa genético Cromosoma Estudio caso Síndrome de genes contiguos Genética Hombre
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling

Discipline
Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16952886

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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