Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10

Molecular Cytogenetics

Volumn 4, Issue 1, 2011, Pages

  Weimer, Jörg ^a   Heidemann, Simone ^a   Von Kaisenberg, Constantin S ^a,b   Grote, Werner ^a   Arnold, Norbert ^a   Bens, Susanne ^a   Caliebe, Almuth ^a  

^a UNIVERSITY OF KIEL   (Germany)

^b HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

array CGH; chromosome microdissection; developmental delay; epicanthus; hypotonia; partial trisomy 7q21.2 7q31.31; short stature; speech delay

Indexed keywords

APGAR SCORE; ARTICLE; CASE REPORT; CHROMOSOME 10; CHROMOSOME 7Q; CHROMOSOME 9P; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME INSERTION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; EAR INFECTION; EPICANTHUS; FACE DYSMORPHIA; FEMALE; FLUORESCENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; GROWTH RETARDATION; HEAD CIRCUMFERENCE; HUMAN; KARYOTYPING; MACROCEPHALY; METACARPOPHALANGEAL JOINT; MICROARRAY ANALYSIS; MICRODISSECTION; MUSCLE HYPOTONIA; PALPEBRAL FISSURE; PARTIAL TRISOMY; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; STRABISMUS; TRISOMY 7; VOMITING;

EID: 82655183758     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-4-28     Document Type: Article

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