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Items: 4

1.
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.
D Warburton
Am J Hum Genet. 1991 Nov; 49(5): 995–1013.
PMCID:
PMC1683246
SummaryPage BrowsePDF–2.5M
2.
Partial trisomy 6q: case report with necropsy findings.
C J Franchino, D Beneck, M A Greco, S R Wolman
J Med Genet. 1987 May; 24(5): 300–303. doi: 10.1136/jmg.24.5.300
PMCID:
PMC1050056
SummaryPage BrowsePDF–770K
3.
The phenotype of ring chromosome 3.
G N Wilson, J Pooley, J Parker
J Med Genet. 1982 Dec; 19(6): 471–473. doi: 10.1136/jmg.19.6.471
PMCID:
PMC1048968
SummaryPage BrowsePDF–557K
4.
Chromosome in situ suppression hybridisation in clinical cytogenetics.
M A Hulten, C P Gould, A S Goldman, J J Waters
J Med Genet. 1991 Sep; 28(9): 577–582. doi: 10.1136/jmg.28.9.577
PMCID:
PMC1015785
SummaryPage BrowsePDF–1.1M

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