Classical and molecular cytogenetic methods in diagnosis of a rare translocation t(3;21).

International journal of molecular medicine

Volumn 1, Issue 3, 1998, Pages 569-571

  Schmitt, H ^a   Sasiadek, M ^a   Jagielski, J ^a   Blin, N ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 21; CHROMOSOME 3; FATHER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETICS; HUMAN; KARYOTYPING; MALE; PREGNANCY; SPONTANEOUS ABORTION;

ABORTION, SPONTANEOUS; ADULT; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 3; FATHERS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PREGNANCY; TRANSLOCATION, GENETIC;

MLCS; MLOWN;

EID: 0032009843     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.1.3.569     Document Type: Article

References (0)