From molecules to behavior: Lessons from the study of rare genetic disorders

Behavior Genetics

Volumn 41, Issue 3, 2011, Pages 341-348

  Roubertoux, Pierre L ^a   De Vries, Petrus J ^b,c  

^a INSERM   (France)

^b CAMBRIDGESHIRE AND PETERBOROUGH NHS FOUNDATION TRUST   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Behavioural phenotypes; diGeorge; Down syndrome; LEOPARD; Neurofibromatosis; Noonan; Rare diseases; Rett; Trisomy 21; Tuberous sclerosis; Williams

Indexed keywords

AMYLOID PRECURSOR PROTEIN; MAMMALIAN TARGET OF RAPAMYCIN; MICRORNA; NEUROLIGIN; NEUROLIGIN 4; PHOSPHATIDYLINOSITOL 3 KINASE; UNCLASSIFIED DRUG;

ALTERNATIVE RNA SPLICING; ALZHEIMER DISEASE; AUTISM; BEHAVIOR DISORDER; BEHAVIOR GENETICS; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; DISEASE ASSOCIATION; FRAGILE X SYNDROME; GENE FUNCTION; GENETIC DISORDER; HUMAN; INTELLECTUAL IMPAIRMENT; LEARNING; LESCH NYHAN SYNDROME; MEMORY; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPIC VARIATION; PREVALENCE; RARE DISEASE; RETT SYNDROME; REVIEW; SEIZURE; TRISOMY 21; TUBEROUS SCLEROSIS;

ANIMALS; DEVELOPMENTAL DISABILITIES; DIGEORGE SYNDROME; DISEASE MODELS, ANIMAL; DOWN SYNDROME; HUMANS; INTELLECTUAL DISABILITY; LEOPARD SYNDROME; MENTAL DISORDERS; MOLECULAR BIOLOGY; NEUROFIBROMATOSES; NOONAN SYNDROME; PHENOTYPE; RARE DISEASES; RETT SYNDROME; TUBEROUS SCLEROSIS; WILLIAMS SYNDROME;

ANIMALIA;

EID: 79958189546     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-011-9469-y     Document Type: Review

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