Skip to main content

. 1967 Dec;4(4):295–298. doi: 10.1136/jmg.4.4.295

An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12).

L J Butler, N E France, N M Jacoby

PMCID: PMC1468560 PMID: 6082910

295

Images in this article

Fig. 1.
on p.295

Fig. 2.
on p.297

Fig. 3.
on p.297

Fig. 4.
on p.298

Selected References

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

BAIN A. D., GAULD I. K. Multiple congenital abnormalities associated with ring chromosome. Lancet. 1963 Aug 10;2(7302):304–305. doi: 10.1016/s0140-6736(63)90212-5. [DOI] [PubMed] [Google Scholar]
Bain A. D., Gauld I. K., Farquhar J. W. A ring X chromosome in dwarfism. Lancet. 1965 Apr 10;1(7389):820–820. doi: 10.1016/s0140-6736(65)92992-2. [DOI] [PubMed] [Google Scholar]
Bishop A. M., Blank C. E., Simpson K., Dewhurst C. J. An XO-X ring X chromosome mosaicism in an individual with normal secondary sexual development. J Med Genet. 1966 Jun;3(2):129–133. doi: 10.1136/jmg.3.2.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
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]
FISHER G. W. RING CHROMOSOME MOSAICISM IN A SEVERELY SUBNORMAL CHILD WITH MULTIPLE CONGENITAL MALFORMATIONS. J Ment Defic Res. 1965 Mar;9:39–50. doi: 10.1111/j.1365-2788.1965.tb00819.x. [DOI] [PubMed] [Google Scholar]
GORDON R. R., COOKE P. RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM. Lancet. 1964 Dec 5;2(7371):1212–1213. doi: 10.1016/s0140-6736(64)91045-1. [DOI] [PubMed] [Google Scholar]
GROPP A., JUSSEN A., OFTERINGER K. MULTIPLE CONGENITAL ANOMALIES ASSOCIATED WITH A PARTIALLY RING-SHAPED CHROMOSOME PROBABLY DERIVED FROM CHROMOSOME NO. 18 IN MAN. Nature. 1964 May 23;202:829–830. doi: 10.1038/202829a0. [DOI] [PubMed] [Google Scholar]
HUSTINX T. W., STOELINGA G. B. A RING-X-CHROMOSOME IN PART OF THE SOMATIC CELLS OF A PATIENT WITH SOME CHARACTERISTICS OF THE TURNER SYNDROME. Genetica. 1964;35:1–14. doi: 10.1007/BF01804870. [DOI] [PubMed] [Google Scholar]
LUCAS M., KEMP N. H., ELLIS J. R., MARSHALL R. A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS. Ann Hum Genet. 1963 Nov;27:189–195. doi: 10.1111/j.1469-1809.1963.tb00212.x. [DOI] [PubMed] [Google Scholar]
PFEIFFER R. A., BUECHNER T. ABSENCE OF LATE REPLICATION OF A HUMAN X-RING CHROMOSOME. Nature. 1964 Nov 21;204:804–805. doi: 10.1038/204804b0. [DOI] [PubMed] [Google Scholar]
Rohde R. A., Tompkins R. "Cri du Chat" due to a ring-B chromosome. Lancet. 1965 Nov 20;2(7421):1075–1076. doi: 10.1016/s0140-6736(65)90609-4. [DOI] [PubMed] [Google Scholar]
SMITH-WHITE S., PEACOCK W. J., TURNER B., DEN DULK G. M. A ring chromosome in man. Nature. 1963 Jan 5;197:102–103. doi: 10.1038/197102b0. [DOI] [PubMed] [Google Scholar]
TURNER B. CYTOGENETIC STUDIES IN MENTAL RETARDATION. Proc Aust Assoc Neurol. 1963 May;72:41–42. [PubMed] [Google Scholar]
WANG H. C., MELNYK J., McDONALD L. T., UCHIDA I. A., CARR D. H., GOLDBERG B. Ring chromosomes in human beings. Nature. 1962 Aug 18;195:733–734. doi: 10.1038/195733a0. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES