Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1971 Jul;23(4):361–367.

Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

F Hecht, W J Kimberling
PMCID: PMC1706712  PMID: 5097902

Full text

PDF
362

Selected References

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

  1. Bauchinger M., Schmid E. Ein Fall mit balancierter (14p+; 15p minus)-Translokation. Humangenetik. 1970;8(4):312–320. doi: 10.1007/BF00280330. [DOI] [PubMed] [Google Scholar]
  2. Cohen M. M., Takagi N., Harrod E. K. Trisomy D1 with two D-D translocation chromosomes. Report of a case. Am J Dis Child. 1968 Feb;115(2):185–190. doi: 10.1001/archpedi.1968.02100010187006. [DOI] [PubMed] [Google Scholar]
  3. De Capoa A., Breg W. R., Kushnick T., Miller O. J. Radioautographic identification of the D chromosomes involved in the centric fusion type of D/G translocation, t(DqGq). Ann Hum Genet. 1968 Oct;32(2):191–193. doi: 10.1111/j.1469-1809.1968.tb00063.x. [DOI] [PubMed] [Google Scholar]
  4. De Capoa A., Rocchi A. Autoradiographic identification of a 13-21 translocation. Cytogenetics. 1970;9(5):396–400. [PubMed] [Google Scholar]
  5. Dekaban A. S. Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation. Am J Hum Genet. 1966 May;18(3):288–295. [PMC free article] [PubMed] [Google Scholar]
  6. Emerit I., Boué J., Dutrillaux B., Prieur M., Lejeune J. Etude autoradiographique de deux translocations t(DqDq) familiales. Ann Genet. 1969 Jun;12(2):94–98. [PubMed] [Google Scholar]
  7. GERMAN J. CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS. Science. 1964 Apr 17;144(3616):298–301. doi: 10.1126/science.144.3616.298. [DOI] [PubMed] [Google Scholar]
  8. Giannelli F., Howlett R. M. The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study. Cytogenetics. 1966;5(3):186–205. doi: 10.1159/000129897. [DOI] [PubMed] [Google Scholar]
  9. Gilgenkrantz S., Grilliat J. P., Vautrin D. A., Plouvier B., Cabrol C. Syndrome 47,XXYY,13-,14-,t(13q14q)+. Ann Genet. 1970 Sep;13(3):201–206. [PubMed] [Google Scholar]
  10. Hecht F., Case M. P., Lovrien E. W., Higgins J. V., Thuline H. C., Melnyk J. Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations. Science. 1968 Jul 26;161(3839):371–372. doi: 10.1126/science.161.3839.371. [DOI] [PubMed] [Google Scholar]
  11. Higurashi M., Matsui I., Nakagome Y., Naganuma M. Down's syndrome: chromosome analysis in 321 cases in Japan. J Med Genet. 1969 Dec;6(4):401–404. doi: 10.1136/jmg.6.4.401. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Higurashi M., Nakagome Y., Nagao T., Naganuma M., Matsui I. Identification of translocated chromosomes by means of autoradiography. Paediatr Univ Tokyo. 1967 Jun;14:14–20. [PubMed] [Google Scholar]
  13. Hsu L. Y., Strauss L., Hirschhorn K. Chromosome abnormality in offspring of LSD user. D trisomy with D-D translocation. JAMA. 1970 Feb 9;211(6):987–990. [PubMed] [Google Scholar]
  14. Krmpotic E., Ramanathan K., Grossman A. A family with D-D translocation. J Med Genet. 1968 Sep;5(3):205–210. doi: 10.1136/jmg.5.3.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lucas M. Translocation between both members of chromosome pair number 15 causing recurrent abortions. Ann Hum Genet. 1969 May;32(4):347–352. doi: 10.1111/j.1469-1809.1969.tb00085.x. [DOI] [PubMed] [Google Scholar]
  16. Léonard A., Deknudt G. A new marker for chromosome studies in the mouse. Nature. 1967 Apr 29;214(5087):504–505. doi: 10.1038/214504a0. [DOI] [PubMed] [Google Scholar]
  17. Mikkelsen M. DNA replication analysis of six 13-15--21 translocation families. Ann Hum Genet. 1967 May;30(4):325–328. doi: 10.1111/j.1469-1809.1967.tb00033.x. [DOI] [PubMed] [Google Scholar]
  18. Mikkelsen M., Niebuhr E. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q). Ann Genet. 1969 Mar;12(1):51–56. [PubMed] [Google Scholar]
  19. Nakagome Y., Bloom A. D. Satellite associations of D group chromosomes in translocation carriers. J Med Genet. 1970 Dec;7(4):371–373. doi: 10.1136/jmg.7.4.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Nakagome Y. DNA replication studies of human D-group chromosomes in satellite associations. Cytogenetics. 1969;8(5):296–303. doi: 10.1159/000130040. [DOI] [PubMed] [Google Scholar]
  21. Neu R. L., Gardner L. I. D-D translocation (XY, D-, t(DqDq)+) in a body with mental retardation and congenital dislocation of the hip. Ann Genet. 1969 Dec;12(4):250–252. [PubMed] [Google Scholar]
  22. Ott J., Robinson A., Peakman D. C. D/D balanced translocations. Lancet. 1968 Dec 21;2(7582):1352–1353. doi: 10.1016/s0140-6736(68)91859-x. [DOI] [PubMed] [Google Scholar]
  23. Palmer C. G., Conneally P. M., Christian J. C. Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p). J Med Genet. 1969 Jun;6(2):166–173. doi: 10.1136/jmg.6.2.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Rowley J. D., Pergament E. Possible non random selection of D group chromosomes involved in centric-fusion translocations. Ann Genet. 1969 Sep;12(3):177–183. [PubMed] [Google Scholar]
  25. SCHMID W. DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES. Cytogenetics. 1963;2:175–193. doi: 10.1159/000129778. [DOI] [PubMed] [Google Scholar]
  26. Sergovich F., Valentine G. H., Chen A. T., Kinch R. A., Smout M. S. Chromosome aberrations in 2159 consecutive newborn babies. N Engl J Med. 1969 Apr 17;280(16):851–855. doi: 10.1056/NEJM196904172801602. [DOI] [PubMed] [Google Scholar]
  27. Sparkes R. S., De Chieri P. R. Inherited 13/14 chromosome translocation as a cause of human fetal wastage. Obstet Gynecol. 1970 Apr;35(4):601–607. [PubMed] [Google Scholar]
  28. Stenchever M. A., Jarvis J. A., Macintyre M. N. Cytogenetics of habitual abortion. Obstet Gynecol. 1968 Oct;32(4):548–555. [PubMed] [Google Scholar]
  29. Vogel W., Höhn H., Engel W. Autoradiographische Identifizierung der an zentrischen Fusionen beteiligten D-Chromosomen bei fünf nichtverwandten Familien: t(14qGq); t(14qGq); t(15qGq); t(13q14q); t(13q15q) Humangenetik. 1970;9(2):140–149. doi: 10.1007/BF00278929. [DOI] [PubMed] [Google Scholar]
  30. Walzer S., Breau G., Gerald P. S. A chromosome survey of 2,400 normal newborn infants. J Pediatr. 1969 Mar;74(3):438–448. doi: 10.1016/s0022-3476(69)80202-7. [DOI] [PubMed] [Google Scholar]
  31. White B. J., Tjio J. H. A mouse translocation with 38 and 39 chromosomes but normal N. F. Hereditas. 1967;58(3):284–296. doi: 10.1111/j.1601-5223.1967.tb02157.x. [DOI] [PubMed] [Google Scholar]
  32. YUNIS J. J., ALTER M., HOOK E. B., MAYER M. FAMILIAL D-D TRANSLOCATION. REPORT OF A PEDIGREE AND DNA REPLICATION ANALYSIS. N Engl J Med. 1964 Nov 26;271:1133–1137. doi: 10.1056/NEJM196411262712203. [DOI] [PubMed] [Google Scholar]
  33. de Grouchy J., Crippa L., German J. Etudes autoradiographiques des chromosomes humains. VII. Cinq observations de t(DqDq) familiales. Ann Genet. 1970 Mar;13(1):19–37. [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES