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Items: 6

1.
Multiplex-FISH for pre- and postnatal diagnostic applications.
S Uhrig, S Schuffenhauer, C Fauth, A Wirtz, C Daumer-Haas, C Apacik, M Cohen, J Müller-Navia, T Cremer, J Murken, M R Speicher
Am J Hum Genet. 1999 Aug; 65(2): 448–462. doi: 10.1086/302508
PMCID:
PMC1377944
SummaryPDF–2.1M
2.
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
A R Zinn, V S Tonk, Z Chen, W L Flejter, H A Gardner, R Guerra, H Kushner, S Schwartz, V P Sybert, D L Van Dyke, J L Ross
Am J Hum Genet. 1998 Dec; 63(6): 1757–1766. doi: 10.1086/302152
PMCID:
PMC1377648
SummaryPDF–262K
3.
Homodicentric chromosomes: a distinctive type of dicentric chromosome.
B E Ward, C M Bradley, J B Cooper, A Robinson
J Med Genet. 1981 Feb; 18(1): 54–58. doi: 10.1136/jmg.18.1.54
PMCID:
PMC1048659
SummaryPage BrowsePDF–673K
4.
Dicentric X isochromosomes in man.
R T Howell, S H Roberts, R J Beard
J Med Genet. 1976 Dec; 13(6): 496–500. doi: 10.1136/jmg.13.6.496
PMCID:
PMC1013476
SummaryPage BrowsePDF–1.1M
5.
An Analysis of the Break Points of Structural Rearrangements in Man
Patricia A. Jacobs, Karin E. Buckton, Catherine Cunningham, Marjorie Newton
J Med Genet. 1974 Mar; 11(1): 50–64. doi: 10.1136/jmg.11.1.50
PMCID:
PMC1013088
SummaryPage BrowsePDF–1.6M
6.
Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes
K. Boczkowski, Margareta Mikkelsen
J Med Genet. 1973 Dec; 10(4): 350–355. doi: 10.1136/jmg.10.4.350
PMCID:
PMC1013055
SummaryPage BrowsePDF–1.5M

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