Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocation.

Journal of medical genetics

Volumn 40, Issue 1, 2003, Pages

  Aboura, A ^a   Labrune, P ^a   Perreaux, F ^a   Poncet, V ^a   Brisset, S ^a   Foix L'Helias, L ^a   Tachdjian, G ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 22; CHROMOSOME 3; CHROMOSOME 9; CHROMOSOME ANALYSIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE TRANSLOCATION; GENETIC RECOMBINATION; GENETICS; HUMAN; INFANT; LETTER; MALE; MEIOSIS; METHODOLOGY; ONCOGENE;

CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 9; CYTOGENETIC ANALYSIS; FEMALE; GENE DELETION; GENES, ABL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MEIOSIS; RECOMBINATION, GENETIC; TRANSLOCATION, GENETIC;

EID: 18344419127     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.1.e6     Document Type: Letter

References (0)