Mutational mechanisms of williams-beuren syndrome deletions

American Journal of Human Genetics

Volumn 73, Issue 1, 2003, Pages 131-151

  Bayés, Mònica ^a   Magano, Luis F ^a   Rivera, Núria ^a   Flores, Raquel ^a   Pérez Jurado, Luis A ^a  

^a UNIVERSITAT POMPEU FABRA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA SUPRAVALVULAR STENOSIS; ARTICLE; CHROMOSOME 7Q; CHROMOSOME BREAKAGE; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; COGNITIVE DEFECT; CROSSING OVER; DNA FLANKING REGION; FACIES; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; GENETIC COUNSELING; HAPLOTYPE; HETEROZYGOSITY; HOMOLOGOUS RECOMBINATION; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; PSEUDOGENE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; STATISTICAL ANALYSIS; WILLIAMS BEUREN SYNDROME;

EID: 0038728033     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/376565     Document Type: Article

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