Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation

Cytogenetic and Genome Research

Volumn 119, Issue 3-4, 2007, Pages 185-190

  Bernheim, A ^a,b   Toujani, S ^a   Guillaud Bataille, M ^a   Richon, C ^b   Waxin, H ^c   Dessen, P ^a,b   Berger, R ^c  

^a UNIVERSITÉ PARIS SACLAY   (France)

^b INSTITUT GUSTAVE ROUSSY   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 6; CHROMOSOME ABERRATION; DNA HYBRIDIZATION; DNA MICROARRAY; FEMALE; GENE DISRUPTION; GENE LOCATION; GENE STRUCTURE; GENE TRANSLOCATION; GENETIC ANALYSIS; HAPLOTYPE; HLA SYSTEM; HUMAN; HUMAN CELL; PHENOTYPE; PRIORITY JOURNAL;

CELL LINE; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 6; DNA; DNA PROBES; FEMALE; GENE DOSAGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TRANSLOCATION, GENETIC;

EID: 39049169628     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000112059     Document Type: Article

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