Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS)

American Journal of Medical Genetics, Part A

Volumn 146, Issue 17, 2008, Pages 2227-2233

  Shriberg, Lawrence D ^a   Jakielski, Kathy J ^b   El Shanti, Hatem ^c  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b AUGUSTANA COLLEGE   (United States)

^c UNIVERSITY OF IOWA   (United States)

Author keywords

Articulatory apraxia; Chromosome translocation; FOXP2; Language disorder; Speech disorder

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR FOXP2; UNCLASSIFIED DRUG;

ADOLESCENT; APRAXIA; ARTICLE; ARTICULATORY APRAXIA; BC087857 GENE; CASE REPORT; CHILDHOOD APRAXIA OF SPEECH; CHROMOSOME 16; CHROMOSOME 4; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DUX4 GENE; DUX4C GENE; DYSARTHRIA; FACE DYSMORPHIA; FAT GENE; FEMALE; FLJ25801 GENE; FLJ38649 GENE; FLUORESCENCE IN SITU HYBRIDIZATION; FRG1 GENE; FRG2 GENE; GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LANGUAGE DISABILITY; MALE; MICROARRAY ANALYSIS; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING; SPEECH ANALYSIS; TRIML1 GENE; TUBB4Q GENE; ZFP42 GENE;

ADOLESCENT; APRAXIAS; CHILD; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SIBLINGS; SPEECH ARTICULATION TESTS; SPEECH DISORDERS; TRANSLOCATION, GENETIC;

EID: 51449089026     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32363     Document Type: Article

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