The neuroanatomy of genetic subtype differences in Prader-Willi syndrome

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 159 B, Issue 2, 2012, Pages 243-253

  Honea, Robyn A ^a   Holsen, Laura M ^b   Lepping, Rebecca J ^c   Perea, Rodrigo ^a   Butler, Merlin G ^a   Brooks, William M ^a,c   Savage, Cary R ^a,c  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

Chromosome 15q; Hyperphagia; MRI; Obesity; Voxel based morphometry

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BODY MASS; BRAIN SIZE; BRAIN STEM; CEREBELLUM; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FRONTAL CORTEX; GENDER; GRAY MATTER; HIPPOCAMPUS; HUMAN; LIMBIC CORTEX; MALE; MIDDLE TEMPORAL GYRUS; NEUROANATOMY; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; ORBITAL CORTEX; PARAHIPPOCAMPAL GYRUS; PARIETAL CORTEX; PHENOTYPE; PRADER WILLI SYNDROME; PREFRONTAL CORTEX; PRIORITY JOURNAL; SCHOOL CHILD; TEMPORAL CORTEX; UNIPARENTAL DISOMY; WHITE MATTER;

ADOLESCENT; ADULT; BRAIN; BRAIN MAPPING; CASE-CONTROL STUDIES; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NEUROANATOMY; NEUROIMAGING; PHENOTYPE; PRADER-WILLI SYNDROME; UNIPARENTAL DISOMY; YOUNG ADULT;

EID: 84855834294     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32022     Document Type: Article

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