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- ARAKAKI D. T., SPARKES R. S. MICROTECHNIQUE FOR CULTURING LEUKOCYTES FROM WHOLE BLOOD. Cytogenetics. 1963;2:57–60. doi: 10.1159/000129767. [DOI] [PubMed] [Google Scholar]
- Atkins L., Feingold M. Enlarged B-group chromosome (4-5). Association with the cri du chat syndrome. Am J Dis Child. 1967 Feb;113(2):277–282. doi: 10.1001/archpedi.1967.02090170141019. [DOI] [PubMed] [Google Scholar]
- Atkins L., Sceery R. T., Keenan M. E. An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development. J Med Genet. 1966 Jun;3(2):134–138. doi: 10.1136/jmg.3.2.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BASRUR P. K., BASRUR V. R., GILMAN J. P. A simple method for short term cultures from small biopsies. Exp Cell Res. 1963 Mar;30:229–232. doi: 10.1016/0014-4827(63)90230-1. [DOI] [PubMed] [Google Scholar]
- BRAY P. F., SISTER ANN JOSEPHINE PARTIAL AUTOSOMAL TRISOMY AND TRANSLOCATION. REPORT OF AN INFANT WITH MULTIPLE CONGENITAL ANOMALIES. JAMA. 1964 Feb 22;187:566–569. [PubMed] [Google Scholar]
- CLARKE G., STEVENSON A. C., DAVIES P., WILLIAMS C. E. A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP. J Med Genet. 1964 Sep;1(1):27–32. doi: 10.1136/jmg.1.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Emery J. L., Kalpaktsoglou P. K. The costochondral junction during later stages of intrauterine life, and abnormal growth patterns found in association with perinatal death. Arch Dis Child. 1967 Feb;42(221):1–13. doi: 10.1136/adc.42.221.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gendel E., Wasserman E. An asymmetric chromosome pair in group 4-5. Association with mental and physical retardation. Am J Dis Child. 1966 Jan;111(1):90–95. doi: 10.1001/archpedi.1966.02090040126018. [DOI] [PubMed] [Google Scholar]
- Gray J. E., Dartnall J. A., Creery R. D., Croudace J. Congenital anomalies due to transmission of a chromosome translocation. J Med Genet. 1966 Mar;3(1):59–61. doi: 10.1136/jmg.3.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hsu L. Y., Nemhauser I., Bettmann H. K., Sobel E. H. Mosaicism of an abnormally long B chromosome in a boy with physical and mental retardation. Pediatrics. 1967 Jan;39(1):68–74. [PubMed] [Google Scholar]
- JACOBSEN P., DUPONT A., MIKKELSEN M. TRANSLOCATION IN THE 13-15 GROUP AS A CAUSE OF PARTIAL TRISOMY AND SPONTANEOUS ABORTION IN THE SAME FAMILY. Lancet. 1963 Sep 14;2(7307):584–585. doi: 10.1016/s0140-6736(63)92673-4. [DOI] [PubMed] [Google Scholar]
- Jensen M. K., Melchior J. C. Possible partial trisomy of a chromosome of group 6-X-12 and familial translocation heterozygosity in a child with congenital abnormalities. Dev Med Child Neurol. 1967 Jun;9(3):313–318. doi: 10.1111/j.1469-8749.1967.tb02275.x. [DOI] [PubMed] [Google Scholar]
- Lejeune J., Burger R. Sur deux observations familiales de translocations complexes. Ann Genet. 1965;8(1):21–30. [PubMed] [Google Scholar]
- MANN J. D., VALDMANIS A., CAPPS S. C., PUITE R. H. A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C. Am J Hum Genet. 1965 Sep;17:377–383. [PMC free article] [PubMed] [Google Scholar]
- Punnet H. H., Pinsky L., Digeorge A. M., Gorlin R. J. Familial reciprocal C/18 translocation. Am J Hum Genet. 1966 Nov;18(6):572–583. [PMC free article] [PubMed] [Google Scholar]
- ROHDE R. A., CATZ B. MATERNAL TRANSMISSION OF A NEW GROUP-C(6/9) CHROMOSOMAL SYNDROME. Lancet. 1964 Oct 17;2(7364):838–840. doi: 10.1016/s0140-6736(64)90688-9. [DOI] [PubMed] [Google Scholar]
- SHAW M. W., COHEN M. M., HILDERBRANDT H. M. A FAMILIAL 4/5 RECIPROCAL TRANSLOCATION RESULTING IN PARTIAL TRISOMY B. Am J Hum Genet. 1965 Jan;17:54–70. [PMC free article] [PubMed] [Google Scholar]
- Thorburn M. J., Miller C. G. Pathology of congenital rubella in Jamaica. Arch Dis Child. 1967 Aug;42(224):389–396. doi: 10.1136/adc.42.224.389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trujillo J. M., Zeller R. S., Plessala R. A., List-Young B. Translocation heterozygosis in man. Am J Hum Genet. 1966 Mar;18(2):215–225. [PMC free article] [PubMed] [Google Scholar]
- Turner J. H., Bass L. W., Kaplan S. Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome. J Med Genet. 1966 Mar;3(1):66–69. doi: 10.1136/jmg.3.1.66. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Grouchy J., Canet J. Translocation 6-12 13-15 et trisomie partielle 6-12 (probablement 10) Ann Genet. 1965;8(1):16–20. [PubMed] [Google Scholar]





