Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2

American Journal of Medical Genetics, Part A

Volumn 146, Issue 13, 2008, Pages 1637-1654

  Dobyns, William B ^a   Mirzaa, Ghayda ^a,b   Christian, Susan L ^a   Petras, Kristin ^a   Roseberry, Jessica ^a,n   Clark, Gary D ^c   Curry, Cynthia J R ^d   McDonald McGinn, Donna ^e   Medne, Livija ^e   Zackai, Elaine ^e   Parsons, Julie ^f   Zand, Dina J ^g   Hisama, Fuki M ^h   Walsh, Christopher A ^h,i   Leventer, Richard J ^j   Martin, Christa L ^k   Gajecka, Marzena ^l   Shaffer, Lisa G ^l,m  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^f UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

^g CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^h BOSTON CHILDREN S HOSPITAL   (United States)

ⁱ HARVARD MEDICAL SCHOOL   (United States)

^j ROYAL CHILDREN'S HOSPITAL   (Australia)

^k EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^l WASHINGTON STATE UNIVERSITY   (United States)

^m Signature Genomic Laboratories LLC   (United States)

ⁿ ELI LILLY AND COMPANY   (United States)

more..

Author keywords

Chromosome 18p; Chromosome 1p36; Chromosome 1q4; Chromosome 21q2; Chromosome 2p; Chromosome 4q2; Chromosome 6q2; Deletion; Duplication; Polymicrogyria

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BRAIN MALFORMATION; CHROMOSOME 18P; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 21Q; CHROMOSOME 2P; CHROMOSOME 4Q; CHROMOSOME 6Q; CHROMOSOME ABERRATION; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CYTOGENETICS; FEMALE; GENE EXPRESSION; GENE LOCATION; GENE LOCUS; GENE MAPPING; HUMAN; HUMAN GENOME; INFANT; MALE; MICROGYRIA; MOLECULAR GENETICS; NEUROIMAGING; NEWBORN; PENETRANCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; ANEUPLOIDY; BRAIN; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; MALFORMATIONS OF CORTICAL DEVELOPMENT; PHENOTYPE; TRANSLOCATION, GENETIC;

EID: 47149093878     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32293     Document Type: Article

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