High resolution snp based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia

American Journal of Medical Genetics, Part A

Volumn 149, Issue 5, 2009, Pages 887-893

  Kogan, Jillene M ^a   Miller, Erin ^a   Ware, Stephanie M ^a,b  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

17p11.2 duplication syndrome; Comparative genomic hybridization; Snp microarray; Supernumerary marker chromosome; Verbal apraxia

Indexed keywords

ANAMNESIS; APRAXIA; ARTICLE; CASE REPORT; CEREBELLUM HYPOPLASIA; CHILD; CHROMOSOME 13; CHROMOSOME 17; CHROMOSOME ABERRATION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE MAPPING; HUMAN; MICROARRAY ANALYSIS; MUSCLE HYPOTONIA; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SUPERNUMERARY CHROMOSOME;

APRAXIAS; CHILD; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 17; DNA MUTATIONAL ANALYSIS; GENETIC MARKERS; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MOSAICISM; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 66849093891     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32750     Document Type: Article

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