The role of RELN in lissencephaly and neuropsychiatric disease

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 144, Issue 1, 2007, Pages 58-63

  Chang, Bernard S ^a,e   Duzcan, Fusun ^b   Kim, Seonhee ^a   Cinbis, Mine ^b   Aggarwal, Abha ^c   Apse, Kira A ^a   Ozdel, Osman ^b   Atmaca, Munevver ^b   Zencir, Sevil ^b   Bagci, Huseyin ^b   Walsh, Christopher A ^d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b PAMUKKALE UNIVERSITY   (Turkey)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

^d BOSTON CHILDREN S HOSPITAL   (United States)

^e NONE   (United States)

Author keywords

Cerebellar hypoplasia; Malformation of cortical development; Pachygyria

Indexed keywords

AGYRIA; ARTICLE; BRAIN DEVELOPMENT; CEREBELLUM HYPOPLASIA; CHROMOSOME 7; CLINICAL ARTICLE; FEMALE; GENE; GENE LOCUS; HUMAN; MALE; MENTAL DISEASE; PARACENTRIC CHROMOSOME INVERSION; PEDIGREE; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; RELN GENE;

BRAIN; CELL ADHESION MOLECULES, NEURONAL; CENTRAL NERVOUS SYSTEM DISEASES; CEREBELLUM; CEREBRAL CORTEX; CHILD; CHROMOSOMES, HUMAN, PAIR 7; CYTOGENETICS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; MAGNETIC RESONANCE IMAGING; MALE; MENTAL DISORDERS; NERVE TISSUE PROTEINS; PEDIGREE; PHENOTYPE; SERINE ENDOPEPTIDASES;

EID: 33846335512     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30392     Document Type: Article

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