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• Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

  Müller H, Bühler EM, Signer E, Egli F, Stalder GR. Müller H, et al. J Med Genet. 1972 Dec;9(4):462-7. doi: 10.1136/jmg.9.4.462. J Med Genet. 1972. PMID: 4646556 Free PMC article. No abstract available.
• Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.

  Tiepolo L, Zuffardi O. Tiepolo L, et al. Hum Genet. 1976 Oct 28;34(2):119-24. doi: 10.1007/BF00278879. Hum Genet. 1976. PMID: 1002136
• Fluorescent staining of human chromosomes: identification of some common aberrations.

  Uchida IA, Lin CC. Uchida IA, et al. Can Med Assoc J. 1971 Sep 4;105(5):479-82. Can Med Assoc J. 1971. PMID: 4106965 Free PMC article.
• A phenotypic male with karyotype 45,X:45,X,ace+(?Yg--).

  Nielsen J, Friedrich U, Christensen AL, Godt HH, Strömgren LS. Nielsen J, et al. Humangenetik. 1972;15(4):319-26. doi: 10.1007/BF00281731. Humangenetik. 1972. PMID: 4634448 No abstract available.
• Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi).

  Ferguson-Smith MA, Boyd E, Ferguson-Smith ME, Pritchard JG, Yusuf AF, Gray B. Ferguson-Smith MA, et al. J Med Genet. 1969 Dec;6(4):422-5. doi: 10.1136/jmg.6.4.422. J Med Genet. 1969. PMID: 5365951 Free PMC article. No abstract available.