Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.

Journal of medical genetics

Volumn 39, Issue 10, 2002, Pages

  Andries, S ^a   Sartenaer, D ^a   Rack, K ^a   Rombout, S ^a   Tuerlinckx, D ^a   Gillerot, Y ^a   Van Maldergem, L ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 19; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENETICS; HUMAN; INFANT; KARYOTYPING; MALE; METHODOLOGY; MICROCEPHALY; NOTE; PSYCHOMOTOR DISORDER; TELOMERE;

CHROMOSOMES, HUMAN, PAIR 19; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MICROCEPHALY; PSYCHOMOTOR DISORDERS; TELOMERE;

MLCS; MLOWN;

EID: 18344407254     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.39.10.e60     Document Type: Note

References (0)