DOUBLE TRANSLOCATION:
AN INTERESTING FAMILY HISTORY
Uysal A1,*, Uludağ A2, Sılan F2, Erçelen N3, Zafer C4, Özdemir Ö2
*Corresponding Author: Assistant Professor Ahmet Uysal, Department of Obstetrics and Gynecology, Çanakkale
Onsekiz Mart University, Çanakkale, Turkey; Tel.: +90-533-263-55-40; Fax: +90-0286-263-59-56; E-mail:
drahmetuysal@hotmail.com
page: 77
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REFERENCES
1. Ward BE, Henry GP, Robinson A. Cytogenetic
studies in 100 couples with recurrent spontaneous
abortions. Am J Hum Genet 1980; 32(4):
549-554.
2. Crolla JA, Youings SA, Ennis S, Jacobs PA.
Super-numerary marker chromosomes in man:
parental origin, mosaicism and maternal age revisited.
Eur J Hum Genet. 2005; 13(2): 154-160.
3. Kochhar PK, Ghosh P. Reproductive outcome of
couples with recurrent miscarriage and balanced
chromo-somal abnormalities. J Obstet Gynaecol
Res. 2013; 39(1): 113-120.
4. Alfarawati S, Fragouli E, Colls P, Wells D. Embryos
of Robertsonian translocation carriers
exhibit a mitotic interchromosomal effect that
enhances genetic instability during early development.
PLoS Genet. 2012; 8(10): e1003025.
doi: 10.1371/journal.pgen.1003025.
5. Ogilvie CM, Braude P, Scriven PN. Successful
pregnancy outcomes after preimplantation
genetic diagnosis (PGD) for carriers of chromosometranslocations.
Hum Fertil (Camb). 2001;
4(3): 168-171.
6. Bowser-Riley SM, Griffiths MJ, Creasy MR,
Farndon PA, Martin KE, Thomson DA, et al.
Are double translocations double trouble? J Med
Genet. 1988; 25(5): 326-331.
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