7q11.23 Deletions in Williams syndrome arise as a consequence of unequal meiotic crossover [1]

American Journal of Human Genetics

Volumn 59, Issue 4, 1996, Pages 958-962

  Urban, Z ^a   Helms, C ^a   Fekete, G ^a   Csiszar, K ^a   Bonnet, D ^a   Munnich, A ^a   Donis Keller, H ^a   Boyd, C D ^a  

^a ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 7Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL EXAMINATION; CROSSING OVER; GENE LOCUS; GENE MAPPING; HAPLOTYPE; HUMAN; LETTER; MEIOSIS; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; CROSSING OVER, GENETIC; GENE DELETION; GENOTYPE; HAPLOIDY; HUMANS; MEIOSIS; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; WILLIAMS SYNDROME;

EID: 0029798778     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)