Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1973.tb01129.x/fullpdf
Reference8 articles.
1. Deleted chromosome 18 with paternal mosaicism;Day;Lancet,1967
2. Familial normal/partial trisomy 16 with selective endoreduplication in malformed proband;Drets;Cytogenetics,1970
3. ABNORMALITIES OF THE AUTOSOMES–GROUP E (16–18 GROUP–DENVER CONFERENCE)
4. Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements;Hecht;Amer. J. hum. Genet.,1971
5. Trisomy 14 in spontaneous abortus;Kajii;Hum. Genet.,1972a
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. On the meaning of fragile sites in cancer risk and development;Cancer Genetics and Cytogenetics;1985-09
2. Fragile chromosome 16(q22) cause a balanced translocation at the same point;Human Genetics;1983-12
3. The fragile site on chromosome 16 (q21q22);Human Genetics;1980-07
4. A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl;Humangenetik;1974-03
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