Follow-up of a familial translocation t(10;16) with an unusual segregation pattern

American Journal of Medical Genetics

Volumn 63, Issue 2, 1996, Pages 363-365

  Resta, Robert G ^a   Luthardt, Frederick ^a   Kapur, Raj ^b  

^a SWEDISH MEDICAL CENTER   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

meiotic drive; segregation distortion; translocation

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 16P; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION 10; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; FOLLOW UP; GENE DISRUPTION; HUMAN; KARYOTYPE 46,XX; MALE; MEIOSIS; PATTERN RECOGNITION; PHENOTYPE; PRIORITY JOURNAL; TRISOMY;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; FOLLOW-UP STUDIES; HUMANS; MALE; PEDIGREE; TRANSLOCATION, GENETIC;

EID: 0030008880     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960517)63:2<363::AID-AJMG7>3.0.CO;2-U     Document Type: Article

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