The 18-Trisomy Syndrome —Two New Clinical Variants
- 2 May 1963
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 268 (18) , 982-988
- https://doi.org/10.1056/nejm196305022681804
Abstract
THE autosomal trisomy syndrome of numerous congenital anomalies associated with a modal chromosome number of 47, the extra chromosome being either number 17 or 18, is now well established.1 Rece-t reports1 2 3 4 have differed in the identification of the extra autosome, some favoring a designation as, number 181 , 2 and some favoring, number 7.3 , 4 Although precise identification is difficult if not impossible, analysis of the idiograms reported below suggested the extra autosome to be number 18. This symptom complex is therefore referred to asromy 18.The sources cited above have agreed, however, on the major systems involved in most of the . . .Keywords
This publication has 13 references indexed in Scilit:
- The No. 18 trisomy syndromeThe Journal of Pediatrics, 1962
- Autosomal trisomy of a group 16–18 chromosomeThe Journal of Pediatrics, 1962
- A case of double trisomy: Trisomy no. 18 and triplo-XThe Journal of Pediatrics, 1962
- A POSSIBLE ASSOCIATION BETWEEN MATERNAL RADIATION AND MONGOLISMThe Lancet, 1961
- A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosomeThe Journal of Pediatrics, 1960
- CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISMThe Lancet, 1960
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVESThe Lancet, 1960
- A MONGOL GIRL WITH 46 CHROMOSOMESThe Lancet, 1960
- An Air-Drying Technique for Flattening Chromosomes in Mammalian Cells GrownIn VitroStain Technology, 1958