A familial complex chromosome translocation resulting in duplication of 6p25

Annales de Genetique

Volumn 47, Issue 3, 2004, Pages 275-280

  Vermeesch, J R ^a   Thoelen, R ^a   Fryns, Jean Pierre ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

Chromosome 6; Deletion; Duplication; Insertional translocation; Subtelomere

Indexed keywords

ARTICLE; CHROMOSOME 12; CHROMOSOME 6P; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GENE DUPLICATION; GENE INSERTION; GENETIC ANALYSIS; HUMAN; MOLECULAR GENETICS; PERICENTRIC CHROMOSOME INVERSION; PSYCHOMOTOR RETARDATION; SPEECH DEVELOPMENT; TELOMERE;

CELLS, CULTURED; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 6; EPILEPSY, TONIC-CLONIC; FACE; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INVERSION, CHROMOSOME; KARYOTYPING; LANGUAGE DEVELOPMENT DISORDERS; LYMPHOCYTES; MENTAL RETARDATION; MUTAGENESIS, INSERTIONAL; PSYCHOMOTOR DISORDERS; TRANSLOCATION, GENETIC; TRISOMY;

INSERTION SEQUENCES;

EID: 4344698996     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anngen.2004.03.002     Document Type: Article

References (12)

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