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Items: 3

1.
Clinical and Molecular Characterization of Patients with Distal 11q Deletions
Laura A. Penny, Marie Dell'Aquila, Marilyn C. Jones, JoAnn Bergoffen, Christopher Cunniff, Jean-Pierre Fryns, Elizabeth Grace, John M. Graham, Boris Kousseff, Teresa Mattina, James Syme, Lucille Voullaire, Leopoldo Zelante, Julie Zenger-Hain, Oliver W. Jones, Glen A. Evans
Am J Hum Genet. 1995 Mar; 56(3): 676–683.
PMCID:
PMC1801184
SummaryPage BrowsePDF–1.5M
2.
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
3.
Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
A J Dawson, A J Mears, A E Chudley, T Bech-Hansen, H McDermid
J Med Genet. 1996 Nov; 33(11): 952–956. doi: 10.1136/jmg.33.11.952
PMCID:
PMC1050791
SummaryPage BrowsePDF–1.4M

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