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Items: 5

1.
Applications of comparative genomic hybridisation in constitutional chromosome studies
C. Breen, L. Barton, A. Carey, A. Dunlop, M. Glancy, K. Hall, A. M. Hegarty, M Khokhar, M. Power, K. Ryan, A. Green, R. Stallings
J Med Genet. 1999 Jul; 36(7): 511–517.
PMCID:
PMC1734415
SummaryPDF–156K
2.
Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndrome
S TAYEL, R AL-NAGGAR, D MURTHY, K NAGUIB, S AL-AWADI, N KARSH
J Med Genet. 1999 May; 36(5): 418–419.
PMCID:
PMC1734370
SummaryPDF–85K
3.
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
4.
The presence of interstitial telomeric sequences in constitutional chromosome abnormalities.
V M Park, K M Gustashaw, T M Wathen
Am J Hum Genet. 1992 May; 50(5): 914–923.
PMCID:
PMC1682611
SummaryPage BrowsePDF–1.9M
5.
Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
H C Duba, M Erdel, J Löffler, L Bereuther, H Fischer, B Utermann, G Utermann
J Med Genet. 1997 Apr; 34(4): 309–313. doi: 10.1136/jmg.34.4.309
PMCID:
PMC1050918
SummaryPage BrowsePDF–1.3M

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