Sequential FISH allows the determination of the segregation outcome and the presence of numerical anomalies in spermatozoa from a t(1;8;2)(q42;p21;p15) carrier

Journal of Assisted Reproduction and Genetics

Volumn 30, Issue 9, 2013, Pages 1115-1123

  Godo, Anna ^a   Blanco, Joan ^a   Vidal, Francesca ^a   Parriego, Mònica ^b   Boada, Montserrat ^b   Anton, Ester ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b INSTITUT UNIVERSITARI DEXEUS   (Spain)

Author keywords

Complex chromosome rearrangement; Fluorescent in situ hybridization; Interchromosomal effect; Meiotic segregation; Spermatozoa

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CENTROMERE; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME REARRANGEMENT; CHROMOSOME SEGREGATION; DIPLOIDY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; GAMETE; HETEROZYGOTE; HUMAN; INTERPHASE; KARYOTYPE 46,XY; KARYOTYPING; MALE; NONDISJUNCTION; PRIMED IN SITU LABELING; PRIORITY JOURNAL; SPERMATOZOON; SPERMATOZOON ABNORMALITY;

ADULT; ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME SEGREGATION; GERM CELLS; HETEROZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MEIOSIS; SPERMATOZOA; TRANSLOCATION, GENETIC;

EID: 84886407781     PISSN: 10580468     EISSN: 15737330     Source Type: Journal    
DOI: 10.1007/s10815-013-0063-5     Document Type: Article

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