Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea

Molecular Human Reproduction

Volumn 3, Issue 5, 1997, Pages 439-443

  Delon, B ^a   Lallaoui, H ^b   Abel Lablanche, C ^b   Geneix, A ^c   Bellec, V ^a   Benkhalifa, M ^a  

^a LMM Laboratoire Marcel Merieux   (France)

^b LABS   (France)

^c Faculté de Médecine   (France)

Author keywords

Secondary amenorrhoea; STS X chromosome; X:Y translocation; Y chromosome

Indexed keywords

DNA;

ADULT; AMENORRHEA; ARTICLE; CASE REPORT; CHROMOSOME BANDING PATTERN; CHROMOSOME MAP; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETIC MARKER; GENETICS; HUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; SEQUENCE TAGGED SITE; X CHROMOSOME; Y CHROMOSOME;

ADULT; AMENORRHEA; CHROMOSOME BANDING; CHROMOSOME MAPPING; DNA; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; SEQUENCE TAGGED SITES; TRANSLOCATION, GENETIC; X CHROMOSOME; Y CHROMOSOME;

EID: 0031137667     PISSN: 13609947     EISSN: None     Source Type: Journal    
DOI: 10.1093/molehr/3.5.439     Document Type: Article

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