Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF02265294.pdf
Reference45 articles.
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2. Abuelo DN, Barsel-Bower S (1988) Two males with amniotic fluid 45,X karyotypes. Am J Hum Genet 43: A224
3. Andersson M, Page DC, Pettay D, Subrt I, Turleau C, Grouchy J de, Chapelle A de la (1988) Y: autosome translocation and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11. Hum Genet 79:2–7
4. Arnemann J, Schnittger S, Hinkel GK, Tolkendorf E, Schmidtke J, Hausmann I (1991) A sterile male with 45,X0 and a Y;22 translocation. Hum Genet 87:134–138
5. Beverstock GC, Macfarlane JD, Veenema H, Hoekman H, Goodfellow PJ (1989) Y chromosome specific probes identify breakpoint in a 45,X/46,X,de1(Y)(pter→ql1.1) karyotype of an infertile male. J Med Genet 26:330–333
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