Summary
A short arm deletion of chromosome No. 15 — del(15)(q11) — was detected in a 13-year-old girl with the clinical diagnosis of anorexia nervosa. The same marker chromosome was also found in the father, who is phenotypically inconspicuous.
Zusammenfassung
Eine Deletion des kurzen Armes des Chromosoms Nr. 15 — del(15) (q11) — wurde bei einem 13jährigen Mädchen mit der klinischen Diagnose Anorexia nervosa gefunden. Die gleiche chromosomale Besonderheit wurde ebenfalls bei dem Vater gefunden, der jedoch phänotypisch unauffällig ist.
References
Bias, W. B., Migeon, B. R.: Haptoglobin: a locus on the A-chromosome. Amer. J. hum. Genet. 19, 393 (1967)
Brogger, A.: Exclution of marker genes from the short arm of the human chromosome D1 by deletion mapping. Hereditas (Lund) 62, 116 (1969)
Burnham, C. R.: Chromosome interchanges in plants. Botan. rev. 22, 419–552 (1956)
Court Brown, W. M.: Human population cytogenetics. Amsterdam: North-Holland Publ. 1967
Court Brown, W. M., Buckton, K. E., Jacobs, P. A., Tough, I. M., Kuenssbergs, E. V., Knox, J. D. E.: Chromosome studies on adults. Eugenics Labo. Mem. No. 42. Galton Labo., Universit College, London: Cambridge Univ. Press 1966
Court Brown, W. M., Jacobs P. A., Buckton, M.: Chromosome studies on randomly chosen men and women. Lancet 1965 II, 561–562
Emerit, I., Grouchy, J., de German, I.: Deletion du bras court d'un chromosome 13. Ann. Génét. 11, 184 (1968)
Emerit, I., Noel, B., Thiriet, M., Loubon, M., Quack, B.: Short arm deletion of chromosome 14. Humangenetik 15, 33–38 (1972)
Grouchy, J., Salmon, Ch., Salmon, D., Maroteaux, P.: Deletion du bras court d'un chromosome 13–15, hypertelerorisme et phénotype haptoglobin HpO dans une même famille. Ann. Génét. 9, 80 (1966)
Lieber, E., Hirschorn, K., Seegers, P., Allderdice, P., Capoa, A., de Miller, O. J.: An anomaly of chromosome 13 in four generations. Abstr. Meet. Amer. Soc. Hum. Genet. toronto, Dec. 1–3 (1967)
Migeon, B. R.: Familial variant autosomes: New human cytogenetics markers. Bull. Johns Hopk. Hosp. 116, 396–402 (1965)
Parker, C. E., Koch, R., Malvalwala, J.: Familial deletion of the short arm of the D1 chromosome not associated with loss of haptoglobin or catalase activity. Clin. Pediat. 8, 453 (1969)
Starman, M. N., Shaw, M. W.: Atypical acrocentric chromosome in Negro and Caucasian Mongols. Amer. J. hum. Genet. 19, 162 (1967)
Wendt, G. G.: A special trial of genetic policlinic. Humangenetic (in press)
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Hoo, J.J., Hillig, U., Cramer, H. et al. Familial short arm deletion of chromosome No. 15. Hum Genet 21, 283–286 (1974). https://doi.org/10.1007/BF00279024
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DOI: https://doi.org/10.1007/BF00279024