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. 1969 Jun;6(2):166–173. doi: 10.1136/jmg.6.2.166

Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p).

C G Palmer, P M Conneally, J C Christian
PMCID: PMC1468862  PMID: 4240722

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Selected References

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

  1. BUHLER E. M., ROSSIER R., BODIS I., VULLIET V., BUHLER U. K., STALDER G. [Chromosomal translocation in a mentally deficient child with cryptorchidism]. Acta Paediatr. 1963 Mar;52:177–182. doi: 10.1111/j.1651-2227.1963.tb03762.x. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. CHAPTAL J., JEAN R., EMBERGER J. M. TRANSLOCATION ENTRE DEUX CHROMOSOMES DU GROUPE 13-15 CHEZ LA M'ERE D'UN MONGOLIEN PAR TRISOMIE 21 R'EGULI'ERE. Arch Fr Pediatr. 1965 Jan;22:35–39. [PubMed] [Google Scholar]
  4. 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]
  5. Conen P. E., Erkman B., Metaxotou C. The "D" syndrome. Report of four trisomic and one D/D translocation case. Am J Dis Child. 1966 Mar;111(3):236–247. doi: 10.1001/archpedi.1966.02090060046002. [DOI] [PubMed] [Google Scholar]
  6. DE GROUCHY J., BRISSAUD H. E., REPESSE G., LAMY M. ANENC'EPHALIE FAMILIALE ET REMANIEMENT DE DEUX CHROMOSOMES 13-15. C R Hebd Seances Acad Sci. 1964 Jul 20;259:691–694. [PubMed] [Google Scholar]
  7. 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]
  8. Engel W., Krone W., Wolf U. Die wirkung von Thioguanin, Hydroxylamin und 5-Bromodesoxyuridin auf menschliche Chromosomen in vitro. Mutat Res. 1967 May-Jun;4(3):353–368. doi: 10.1016/0027-5107(67)90030-9. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Grell R. F. Pairing at the chromosomal level. J Cell Physiol. 1967 Oct;70(2 Suppl):119–146. doi: 10.1002/jcp.1040700410. [DOI] [PubMed] [Google Scholar]
  11. HAMERTON J. L., GIANNELLI F., CARTER C. O. A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME. Cytogenetics. 1963;2:194–207. doi: 10.1159/000129779. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Hemet J., Lamachère D., Forthomme J., Ensel J. Trisomie 13 par aberration de structure. Ann Anat Pathol (Paris) 1967 Jan-Mar;12(1):101–104. [PubMed] [Google Scholar]
  14. JAGIELLO G. M. Familial 13-15 translocation abnormality (Denver classification) associated with one case of cerebral palsy. Preliminary report. N Engl J Med. 1963 Jul 11;269:66–69. doi: 10.1056/NEJM196307112690202. [DOI] [PubMed] [Google Scholar]
  15. JONGBLOET P., VANWINCKEL H., ANDRIAENSSENS K., HOOFT C. SPORADIC TRISOMY D1 WITH TRANSLOCATION D-D. Helv Paediatr Acta. 1964 Jul;19:121–126. [PubMed] [Google Scholar]
  16. Jacobsen P., Mikkelsen M., Froland A., Dupont A. Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies. Ann Hum Genet. 1966 May;29(4):391–402. doi: 10.1111/j.1469-1809.1966.tb00537.x. [DOI] [PubMed] [Google Scholar]
  17. KJESSLER B. MEIOSIS IN A MAN WITH A D/D TRANSLOCATION AND CLINICAL STERILITY. Lancet. 1964 Jun 27;2(7348):1421–1423. doi: 10.1016/s0140-6736(64)91989-0. [DOI] [PubMed] [Google Scholar]
  18. Marsden H. B., Mackay R. I., Murray A., Ward H. E. Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome. J Med Genet. 1966 Mar;3(1):56–58. doi: 10.1136/jmg.3.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Orye E., Delire C. Familial D/D and D/G, translocation. Helv Paediatr Acta. 1967 Apr;22(1):36–40. [PubMed] [Google Scholar]
  20. PITT D., FERGUSON J., BAIKIE A. G. NORMAL AND ABNORMAL SIBS WITH A FAMILIAL CHROMOSOMAL TRANSLOCATION. Australas Ann Med. 1964 May;13:178–182. doi: 10.1111/imj.1964.13.2.178. [DOI] [PubMed] [Google Scholar]
  21. Palmer C. G., Funderburk S. Secondary constrictions in human chromosomes. Cytogenetics. 1965;4(4):261–276. doi: 10.1159/000129863. [DOI] [PubMed] [Google Scholar]
  22. Pinkerton P. H., Cohen M. M. Persistence of hemoglobin F in D/D translocation with trisomy 13-15 (D1). JAMA. 1967 May 15;200(7):647–649. [PubMed] [Google Scholar]
  23. Summitt R. L., Atnip R. L. Chromosomal aberrations with normal phenotype: four examples. Ala J Med Sci. 1966 Oct;3(4):483–487. [PubMed] [Google Scholar]
  24. Tolksdorf M., Wiedemann H. R., Hansen H. G., Lehmann W. Pätau-Syndrom mit Trisomie D 1 und D/D -Translokation. Med Welt. 1965 Oct 9;41:2304–2307. [PubMed] [Google Scholar]
  25. 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]
  26. ZERGOLLERN L., HOEFNAGEL D., BENIRSCHKE K., CORCORAN P. A. A PATIENT WITH TRISOMY 21 AND A RECIPROCAL TRANSLOCATION IN THE 13-15 GROUP. Cytogenetics. 1964;3:148–158. doi: 10.1159/000129806. [DOI] [PubMed] [Google Scholar]
  27. de GROUCHY, MLYNARSKI J. C., MAROTEAUX P., LAMYM, DESHAIES G., BENICHOU C., SALMON C. [Polydysspondylic syndrome due to 14-15 translocation and dyschondrosteosis in the same subject. Familial segregation]. C R Hebd Seances Acad Sci. 1963 Feb 11;256:1614–1616. [PubMed] [Google Scholar]

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