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. 1968 Mar;20(2):107–118.

Familial occurrence of trisomy 22.

I A Uchida, M Ray, K N McRae, D F Besant

PMCID: PMC1706268 PMID: 5643178

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Antich J., Ribas-Mundo M., Prats J., Frances J. M. XO-XX-XXX mosaicism with Turner stigmata. Lancet. 1967 Jun 3;1(7501):1228–1229. doi: 10.1016/s0140-6736(67)92880-2. [DOI] [PubMed] [Google Scholar]
Brown W. M., Jacobs P. A., Brunton M. Chromosome studies on randomly chosen men and women. Lancet. 1965 Sep 18;2(7412):561–562. doi: 10.1016/s0140-6736(65)90867-6. [DOI] [PubMed] [Google Scholar]
Crawfurd M. D., Lele K. P. A child with an extra small metacentric chromosome. Ann Hum Genet. 1965 Nov;29(2):199–205. doi: 10.1111/j.1469-1809.1965.tb00514.x. [DOI] [PubMed] [Google Scholar]
DELACHAPELLE A., AULA P., KIVALO E. ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER. Cytogenetics. 1963;2:129–139. doi: 10.1159/000129774. [DOI] [PubMed] [Google Scholar]
FERGUSON J., PITT D. Another child with 47 chromosomes. Med J Aust. 1963 Apr 13;50(1):546–547. [PubMed] [Google Scholar]
GUSTAVSON K. H., HAGBERG B., FINLEY S. C., FINLEY W. H. An apparently identical extra autosome in two severely retarded sisters with multiple malformations. Cytogenetics. 1962;1:32–41. doi: 10.1159/000129711. [DOI] [PubMed] [Google Scholar]
Giorgi P. L., Paci A., Ceccarelli M. An extra chromosome in a case of Tay-Sachs disease with additional abnormalities. Helv Paediatr Acta. 1967 Apr;22(1):28–35. [PubMed] [Google Scholar]
ISHMAEL J., LAURENCE K. M. A PROBABLE CASE OF INCOMPLETE TRISOMY OF A CHROMOSOME OF THE 13-15 GROUP. J Med Genet. 1965 Jun;2(2):136–141. doi: 10.1136/jmg.2.2.136. [DOI] [PMC free article] [PubMed] [Google Scholar]
KOULISCHER L., PERIER J. [Apropos of a case of 22-trisomy]. Bull Acad R Med Belg. 1962;2:329–344. [PubMed] [Google Scholar]
MOSS M. H., SAPHIRL R., GOTTLIEB M. I. MANDIBULOFACIAL DYSOSTOSIS. REPORT OF TWO CASES WITH CHROMOSOME ANALYSIS. Am J Dis Child. 1964 Mar;107:304–307. [PubMed] [Google Scholar]
McKenzie J. The first arch syndrome. Dev Med Child Neurol. 1966 Feb;8(1):55–66. doi: 10.1111/j.1469-8749.1966.tb08273.x. [DOI] [PubMed] [Google Scholar]
ROTHFELS K. H., SIMINOVITCH L. An air-drying technique for flattening chromosomes in mammalian oells grown in vitro. Stain Technol. 1958 Mar;33(2):73–77. doi: 10.3109/10520295809111827. [DOI] [PubMed] [Google Scholar]
SCHACHENMANN G., SCHMID W., FRACCARO M., MANNINI A., TIEPOLO L., PERONA G. P., SARTORI E. CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA. Lancet. 1965 Aug 7;2(7406):290–290. doi: 10.1016/s0140-6736(65)92415-3. [DOI] [PubMed] [Google Scholar]
SCHMID W. A familial chromosome abnormality associated with repeated abortions. Cytogenetics. 1962;1:199–209. doi: 10.1159/000129729. [DOI] [PubMed] [Google Scholar]
SCHMID W. DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES. Cytogenetics. 1963;2:175–193. doi: 10.1159/000129778. [DOI] [PubMed] [Google Scholar]
YUNIS J. J., HOOK E. B., MAYER M. IDENTIFICATION OF THE MONGOLISM CHROMOSOME BY DNA REPLICATION ANALYSIS. Am J Hum Genet. 1965 May;17:191–201. [PMC free article] [PubMed] [Google Scholar]

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