Deletion of exons 1a-2 of BRCA1: a rather frequent pathogenic abnormality.

Genetic testing and molecular biomarkers

Volumn 13, Issue 3, 2009, Pages 399-406

  van den Ouweland, Ans M W ^a   Dinjens, Winand N M ^a   Dorssers, Lambert C J ^a   van Veghel Plandsoen, Monique M ^a   Brüggenwirth, Hennie T ^a   Withagen Hermans, Caroline J ^a   Collée, Johanna Margriet ^a   Joosse, Simon A ^a   Terlouw Kromosoeto, Joan N R ^a   Nederlof, Petra M ^a  

^a JOSEPHINE NEFKENS INSTITUTE   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; BREAST TUMOR; COHORT ANALYSIS; DNA SEQUENCE; EXON; FAMILY; FEMALE; GENE DELETION; GENETIC MARKER; GENETICS; HAPLOTYPE; HETEROZYGOSITY LOSS; HUMAN; INTRON; ISOLATION AND PURIFICATION; MIDDLE AGED; NUCLEIC ACID AMPLIFICATION; NUCLEIC ACID HYBRIDIZATION; OVARY TUMOR; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; TUMOR SUPPRESSOR GENE;

ADULT; BREAST NEOPLASMS; COHORT STUDIES; DNA, NEOPLASM; EXONS; FAMILY; FEMALE; GENES, BRCA1; GENETIC MARKERS; HAPLOTYPES; HUMANS; INTRONS; LOSS OF HETEROZYGOSITY; MIDDLE AGED; NUCLEIC ACID AMPLIFICATION TECHNIQUES; NUCLEIC ACID HYBRIDIZATION; OVARIAN NEOPLASMS; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 67651056140     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2008.0155     Document Type: Article

References (0)