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22q13.3 Deletion Syndrome : A Recognizable Malformation Syndrome Associated With Marked Speech and Language Delay

Author
CUSMANO-OZOG, Kristina1 ; MANNING, Melanie A2 ; HOYME, H. Eugene3
[1] Stanford UCSF Medical Genetics Program, United States
[2] Stanford University School of Medicine, United States
[3] Department of Pediatrics at the Sanford School of Medicine of the University of South Dakota, United States
Issue title
Subtelomeric microdeletion Syndromes
Author (monograph)
SPINNER, Nancy B (Editor)1 2 ; KRANTZ, Ian D (Editor)1 2
[1] University of Pennsylvania, United States
[2] Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia PA, United States
Source

American journal of medical genetics. Part C, Seminars in medical genetics. 2007, Vol 145, Num 4, pp 393-398, 6 p ; ref : 3/4 p

ISSN
1552-4868
Scientific domain
Genetics
Publisher
Wiley-Liss, Hoboken, NJ
Publication country
United States
Document type
Article
Language
English
Author keyword
autism chromosome anomaly deletion 22q13.3 developmental disabilities dysmorphology speech and language delay terminal 22q deletion syndrome
Keyword (fr)
Anomalie Association Autisme Chromosome G22 Dysmorphie Délétion Malformation Retard langage Syndrome Terminal Trouble du développement Trouble neurologique Aberration chromosomique Pathologie du système nerveux
Keyword (en)
Anomaly Association Autism Chromosome G22 Dysmorphism Deletion Malformation Language retardation Syndrome Terminal Developmental disorder Neurological disorder Chromosomal aberration Nervous system diseases
Keyword (es)
Anomalía Asociación Autismo Cromosoma G22 Dismorfia Deleción Malformación Retardo lenguaje Síndrome Terminal Trastorno desarrollo Trastorno neurológico Aberración cromosómica Sistema nervioso patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B18 Psychopathology. Psychiatry / 002B18D Child clinical studies / 002B18D04 Developmental disorders / 002B18D04B Infantile autism

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics

Francis
770 Psychology. Psychoanalysis. Psychiatry / 770-D Psychopathology. Psychiatry / 770-D04 Child clinical studies / 770-D04D Developmental disorders / 770-D04D02 Infantile autism

Discipline
Medical genetics Psychopathology. Psychiatry. Clinical psychology
Origin
Inist-CNRS
Database
FRANCIS ; PASCAL
INIST identifier
19889115

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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