A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27

American Journal of Medical Genetics, Part A

Volumn 146, Issue 9, 2008, Pages 1151-1157

  Santos, Neide F ^a   Secolin, Rodrigo ^a   Brandão Almeida, Iara L ^a   Silva, Marilza S ^a   Torres, Fábio R ^a   Tsuneda, Simone S ^a   Guimarães, Catarina A ^a   Hage, Simone R V ^b   Cendes, Fernando ^a   Guerreiro, Marilisa M ^a   Lopes Cendes, Iscia ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Cortical malformation; Linkage analysis; X linked inheritance

Indexed keywords

ADULT; ARTICLE; CENTROMERE; CHROMOSOME MAP; CHROMOSOME XQ; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CLINICAL EXAMINATION; COMPUTER PROGRAM; EPILEPSY; FAMILY STUDY; FEMALE; GENE LOCUS; GENOTYPE; HAPLOTYPE; HUMAN; LINKAGE ANALYSIS; MALE; MENTAL DEFICIENCY; MICROGYRIA; MICROSATELLITE MARKER; NEUROIMAGING; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SUPRASYLVIAN GYRUS; X CHROMOSOME LINKED DISORDER;

ADULT; CEREBRAL CORTEX; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, X; FEMALE; GENOTYPE; HAPLOTYPES; HUMANS; LOD SCORE; MAGNETIC RESONANCE IMAGING; MALE; MALFORMATIONS OF CORTICAL DEVELOPMENT; MICROSATELLITE REPEATS; PEDIGREE;

EID: 43049095680     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32270     Document Type: Article

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