A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: Molecular characterization and segregation analysis in male meiosis

Cytogenetic and Genome Research

Volumn 98, Issue 1, 2002, Pages 1-8

  Trappe, R ^a   Bohm D ^a   Kohlhase, J ^a   Weise, A ^b   Liehr, T ^b   Essers, G ^a   Meins, M ^a   Zoll, B ^a   Bartels, I ^a   Burfeind, P ^a,c  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^c Institute of Human Genetics   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILDBIRTH; CHROMOSOME 2; CHROMOSOME 20; CHROMOSOME SEGREGATION; CONGENITAL MALFORMATION; FAMILY; FEMALE; FETUS; FETUS WASTAGE; GENE FREQUENCY; GENETIC RISK; HETEROZYGOTE; HUMAN; MALE; MEIOSIS; MONOSOMY; PARTIAL TRISOMY; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; RECURRENT ABORTION; SPERMATOZOON; CASE REPORT; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETICS; GENOME IMPRINTING; KARYOTYPING; PEDIGREE; PREGNANCY; REVIEW;

ABORTION, HABITUAL; ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MEIOSIS; PEDIGREE; PREGNANCY; TRANSLOCATION, GENETIC;

EID: 0036982615     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000068533     Document Type: Article

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