Homozygosity for a Y/22 chromosome translocation: t(Y;22) (q12;p12/13)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb00820.x/fullpdf
Reference12 articles.
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2. Use of repetitive DNA for diagnosis of chromosomal rearrangements;Burk;Hum. Genet.,1983
3. The identification of Y chromosome translocations following Di-stamycin-A treatment;Cohen;Clin. Genet.,1981
4. Confirmation of Y/autosome translocations using recombinant DNA;Cooke;Hum. Genet.,1979
5. Characterisation of a human Y-chro-mosome repeated sequence and related sequences in higher primates;Cooke;Chromosoma,1982
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1. An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization;Journal of Assisted Reproduction and Genetics;2018-06-02
2. A homozygous balanced reciprocal translocation suggestsLINC00237as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome;American Journal of Medical Genetics Part A;2012-10-03
3. Homozygosity for constitutional chromosomal rearrangements: a systematic review with reference to origin, ascertainment and phenotype;Journal of Human Genetics;2010-06-24
4. Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment;Human Molecular Genetics;2008-11-20
5. Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity;American Journal of Medical Genetics Part A;2006
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