Full text
PDF











Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- CARR D. H. Chromosomal abnormalities and their relation to disease. Can Med Assoc J. 1963 Mar 2;88:456–461. [PMC free article] [PubMed] [Google Scholar]
- CHANDRA H. S., HUNGERFORD D. A. AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL. Cytogenetics. 1963;2:34–41. doi: 10.1159/000129763. [DOI] [PubMed] [Google Scholar]
- COOPER H. L., HIRSCHHORN K. Enlarged satellites as a familial chromosome marker. Am J Hum Genet. 1962 Jun;14:107–124. [PMC free article] [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]
- DEKABAN A. S., BENDER M. A., ECONOMOS G. E. CHROMOSOME STUDIES IN MONGOLOIDS AND THEIR FAMILIES. Cytogenetics. 1963;2:61–75. doi: 10.1159/000129768. [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]
- ELLIS J. R., PENROSE L. S. Enlarged satellites and multiple malformations in the same pedigree. Ann Hum Genet. 1961 Oct;25:159–162. doi: 10.1111/j.1469-1809.1961.tb01514.x. [DOI] [PubMed] [Google Scholar]
- FERGUSON-SMITH M. A., FERGUSON-SMITH M. E., ELLIS P. M., DICKSON M. The sites and relative frequencies of secondary constrictions in human somatic chromosomes. Cytogenetics. 1962;1:325–343. doi: 10.1159/000129743. [DOI] [PubMed] [Google Scholar]
- FERGUSON-SMITH M. A., HANDMAKER S. D. THE ASSOCIATION OF SATELLITED CHROMOSOMES WITH SPECIFIC CHROMOSOMAL REGIONS IN CULTURED HUMAN SOMATIC CELLS. Ann Hum Genet. 1963 Nov;27:143–156. doi: 10.1111/j.1469-1809.1963.tb00207.x. [DOI] [PubMed] [Google Scholar]
- GRAY J. E., MUTTON D. E., ASHBY D. W. Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism. Lancet. 1962 Jan 6;1(7219):21–23. doi: 10.1016/s0140-6736(62)92643-0. [DOI] [PubMed] [Google Scholar]
- HAMERTON J. L., GIANNELLI F., POLANI P. E. CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS. Cytogenetics. 1965;4:171–185. doi: 10.1159/000129853. [DOI] [PubMed] [Google Scholar]
- HANDMAKER S. D. The satellited chromosomes of man with reference to the marfan syndrome. Am J Hum Genet. 1963 Mar;15:11–18. [PMC free article] [PubMed] [Google Scholar]
- HARNDEN D. G. A human skin culture technique used for cytological examinations. Br J Exp Pathol. 1960 Feb;41:31–37. [PMC free article] [PubMed] [Google Scholar]
- JACOBSON T. S., TISCHLER B., MILLER J. R. ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS. Ann Hum Genet. 1964 Sep;28:21–26. doi: 10.1111/j.1469-1809.1964.tb00456.x. [DOI] [PubMed] [Google Scholar]
- JACOBS P. A., BRUNTON M., BROWN W. M. CYTOGENETIC STUDIES IN LEUCOCYTES ON THE GENERAL POPULATION: SUBJECTS OF AGES 65 YEARS AND MORE. Ann Hum Genet. 1964 Jun;27:353–365. doi: 10.1111/j.1469-1809.1963.tb01532.x. [DOI] [PubMed] [Google Scholar]
- KALLEN B., LEVAN A. Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome. Cytogenetics. 1962;1:5–19. doi: 10.1159/000129709. [DOI] [PubMed] [Google Scholar]
- MILLER O. R., MUKHERJEE B. B., BREG W. R. Normal variations in the human karyotype. Trans N Y Acad Sci. 1962 Feb;24:372–382. doi: 10.1111/j.2164-0947.1962.tb01413.x. [DOI] [PubMed] [Google Scholar]
- MOORHEAD P. S., MELLMAN W. J., WENAR C. A familial chromosome translocation associated with speech and mental retardation. Am J Hum Genet. 1961 Mar;13:32–46. [PMC free article] [PubMed] [Google Scholar]
- MOORHEAD P. S., NOWELL P. C., MELLMAN W. J., BATTIPS D. M., HUNGERFORD D. A. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res. 1960 Sep;20:613–616. doi: 10.1016/0014-4827(60)90138-5. [DOI] [PubMed] [Google Scholar]
- Moores E. C., Anders J. M., Emanuel R. Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease. Ann Hum Genet. 1966 Jul;30(1):77–84. doi: 10.1111/j.1469-1809.1966.tb00008.x. [DOI] [PubMed] [Google Scholar]
- OHNO S., TRUJILLO J. M., KAPLAN W. D., KINOSITA R. Nucleolus-organisers in the causation of chromosomal anomalies in man. Lancet. 1961 Jul 15;2(7194):123–126. doi: 10.1016/s0140-6736(61)92647-2. [DOI] [PubMed] [Google Scholar]
- PATAU K., THERMAN E., SMITH D. W., INHORN S. L., PICKEN B. F. Partial-trisomy syndromes. I. Sturge-Weber's disease. Am J Hum Genet. 1961 Sep;13:287–298. [PMC free article] [PubMed] [Google Scholar]
- SAKSELA E., MOORHEAD P. S. Enhancement of secondary constrictions and the heterochromatic X in human cells. Cytogenetics. 1962;1:225–244. doi: 10.1159/000129733. [DOI] [PubMed] [Google Scholar]
- SASAKI M. S., MAKINO S. The demonstration of secondary constrictions in human chromosomes by means of a new technique. Am J Hum Genet. 1963 Mar;15:24–33. [PMC free article] [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]
- Starkman M. N., Shaw M. W. Atypical acrocentric chromosomes in Negro and Caucasian Mongols. Am J Hum Genet. 1967 Mar;19(2):162–173. [PMC free article] [PubMed] [Google Scholar]
- THERKELSEN A. J. ENLARGED SHORT ARM OF A SMALL ACROCENTRIC CHROMOSOME IN GRANDFATHER, MOTHER AND CHILD, THE LATTER WITH DOWN'S SYNDROME. Cytogenetics. 1964;3:441–451. doi: 10.1159/000129832. [DOI] [PubMed] [Google Scholar]
- Tjio J. H., Puck T. T., Robinson A. THE HUMAN CHROMOSOMAL SATELLITES IN NORMAL PERSONS AND IN TWO PATIENTS WITH MARFAN'S SYNDROME. Proc Natl Acad Sci U S A. 1960 Apr;46(4):532–539. doi: 10.1073/pnas.46.4.532. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Uchida I. A., Ray M., McRae K. N., Besant D. F. Familial occurrence of trisomy 22. Am J Hum Genet. 1968 Mar;20(2):107–118. [PMC free article] [PubMed] [Google Scholar]
- WOLF U., BAITSCH H., KUENZER W., REINWEIN H. FAMILIAERES AUFTRETEN EINES ANOMALEN D-CHROMOSOMS. Cytogenetics. 1964;3:112–123. doi: 10.1159/000129802. [DOI] [PubMed] [Google Scholar]