Author:
Spiteri E.,Babcock M.,Kashork C. D.,Wakui K.,Gogineni S.,Lewis D. A.,Williams K. M.,Minoshima S.,Sasaki T.,Shimizu N.,Potocki L.,Pulijaal V.,Shanske A.,Shaffer L. G.,Morrow B. E.
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Cited by
46 articles.
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1. Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study;International Journal of Cancer;2019-01-11
2. Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities;American Journal of Medical Genetics Part A;2017-12
3. Complexity of a small non-protein coding sequence in chromosomal region 22q11.2: presence of specialized DNA secondary structures and RNA exon/intron motifs;BMC Genomics;2015-10-14
4. Distinct karyotypes in two offspring of a man with jumping translocation karyotype 45,XY,der(16)t(16;22)(q24;q11.2), −22 [59]/45,XY,der(1)t(1;22)(p36;q11.2), −22 [11]/45,XY,der(22)t(22;22)(p13;q11.2), −22 [10];American Journal of Medical Genetics Part A;2014-04-15
5. Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer;Cancer Genetics;2012-11