Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1970 Jun;7(2):142–147. doi: 10.1136/jmg.7.2.142

Significance of chromosome 17ps+ in three generations of a family.

J H Priest, D C Peakman, S R Patil, A Robinson
PMCID: PMC1468801  PMID: 5519600

Full text

PDF
142

Images in this article

Selected References

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

  1. Berg J. M., Faunch J. A., Pendrey M. J., Penrose L. S., Ridler M. A., Shapiro A. A homozygous chromosomal variant. Lancet. 1969 Mar 8;1(7593):531–531. doi: 10.1016/s0140-6736(69)91627-4. [DOI] [PubMed] [Google Scholar]
  2. Donahue R. P., Bias W. B., Renwick J. H., McKusick V. A. Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc Natl Acad Sci U S A. 1968 Nov;61(3):949–955. doi: 10.1073/pnas.61.3.949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Emerit I., de Grouchy J., Vernant P., Corone P. Chromosomal abnormalities and congenital heart disease. Circulation. 1967 Dec;36(6):886–905. doi: 10.1161/01.cir.36.6.886. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. FERGUSON-SMITH M. A., HANDMAKER S. D. Observations on the satellited human chromosomes. Lancet. 1961 Mar 25;1(7178):638–640. doi: 10.1016/s0140-6736(61)91655-5. [DOI] [PubMed] [Google Scholar]
  6. German J., Ehlers K. H., Engle M. A. Familial congenital heart disease. II. Chromosomal studies. Circulation. 1966 Sep;34(3):517–523. doi: 10.1161/01.cir.34.3.517. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. McGavin D. D., Cant J. S., Ferguson-Smith M. A., Ellis P. M. The cri-du-chat syndrome with an apparently normal karyotype. Lancet. 1967 Aug 12;2(7511):326–330. doi: 10.1016/s0140-6736(67)90170-5. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Schmid E., Bauchinger M. Structural polymorphism in chromosome 17. Nature. 1969 Jan 25;221(5178):387–388. doi: 10.1038/221387a0. [DOI] [PubMed] [Google Scholar]
  11. Therkelsen A. J., Lamm L. U. Heritable morphological difference between the two chromosomes no. 16 in humans. Hereditas. 1967;57(1):149–158. doi: 10.1111/j.1601-5223.1967.tb02097.x. [DOI] [PubMed] [Google Scholar]
  12. Tjio J. H., Puck T. T., Robinson A. THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTS. Proc Natl Acad Sci U S A. 1959 Jul;45(7):1008–1016. doi: 10.1073/pnas.45.7.1008. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES