FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure

Clinical Genetics

Volumn 50, Issue 4, 1996, Pages 267-269

  Riva, P ^a   Magnani, I ^a   Fuhrmann Conti, A M ^a   Gelli, D ^b   Sala, C ^c   Toniolo, D ^c,d   Larizza, L ^a,e  

^a UNIVERSITY OF MILAN   (Italy)

^b OSPEDALE NIGUARDA CA GRANDA   (Italy)

^c San Raffaele Scientific Institute   (Italy)

^d CNR   (Italy)

^e Dipto Biol Genet le Sci Mediche   (Italy)

Author keywords

FISH; Ovarian failure; X autosome translocation

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; OVARY INSUFFICIENCY; PRIORITY JOURNAL;

EID: 0030443546     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02642.x     Document Type: Article

References (9)

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