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Original Article

The influence of sex chromosomes on finger dermatoglyphic patterns

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Pages 287-295 | Received 29 Jul 1985, Published online: 09 Jul 2009

References

  • Alter M. Is hyperploidy of sex chromosomes associated with reduced finger ridge count?. American Journal of Physical Anthropology 1965; 17: 473–475
  • Alvesalo L., Tammisalo E. Enamel thickness in 45,X females' permanent teeth. American Journal of Human Genetics 1981; 33: 464–469
  • Aue-Hauser G. Fingerbeerenmuster und quantitative Werte von 1000 und 1000 Wienern. Mitteilungen der Anthropologischen Gesellschaft in Wien 1976; 106: 126–141
  • Barlow P. The influence of inactive chromosomes on human development. Humangenetik 1973; 17: 105–136
  • Bener A. Sex differences and bilateral asymmetry in dermatoglyphic pattern elements on the finger tips. Annals of Human Genetics 1979; 42: 333–342
  • Cunha G.R., Shannon J.M., Neubauer B.L., Saywer L.M., Fujii H., Taguchi O., Chung L.W.K. Mesechymal-epithelial interactions in sex differentiation. Human Genetics 1981; 58: 68–77
  • Geschwind N., Behan P. Left-handedness: Association with immune disease, migraine, and developmental learning disorder. Proceedings of the National Academy of Sciences 1982; 79: 5097–5100
  • Holt S. The Genetics of Dermal Ridges. Charles C. Thomas, Springfield 1968
  • Holt S., Lindsten J. Dermatoglyphic anomalies in Turner's syndrome. Annals of Human Genetics 1964; 28: 87–100
  • Jantz R.L., Raynard G.C., Owsley D.W. Finger ridge-count variation in 45,X Turner syndrome. Human Genetics 1981; 57: 376–379
  • Jantz R.L., Owsley D.W. Factor analysis of finger ridge counts in Blacks and Whites. Annals of Human Biology 1977; 4: 357–366
  • Jantz R.L., Parham K.R. Some developmental implications of size corrected finger ridge-count correlations. American Journal of Physical Anthropology 1981; 54: 236–237
  • Jantz R.L., Webb R.S. The influence of sex chromosomes and race on asymmetry of finger ridge-counts. American Journal of Physical Anthropology 1980; 52: 241–241
  • Kerr J.M., Hsu L.Y.F., Workman P., Hirschhorn K. Total finger ridge-count and 45,X mosaicism (with and without Y chromosome). Clinical Genetics 1974; 5: 68–71
  • Loesch D. Quantitative Dermatoglyphics: Classification, genetics and pathology. Oxford University Press, Oxford 1983
  • Lyon M., Cattanach B., Charlton H. Genes affecting sex differentiation in mammals. Mechanism of Sex Differentiation in Animals and Man. Acadmic Press, London, New York 1981; 329–386, In
  • Martin N., Jinks J., Berry H., Loesch D. A genetical analysis of diversity and asymmetry in finger ridge-counts. Heredity 1982; 48: 393–405
  • Mittwoch U., Mahadevaiah S. Additional growth—A link between mammalian testes, avian ovaries, gonadal asymmetry in hermaphrodites and the expression of H-Y antigen. Growth 1980; 44: 287–300
  • Oliveira L.L. Dermatoglyphics of University of Tennessee students: relationships to height, weight, laterality and genetic polymorphisms. Thesis. University of Tennessee, Knoxville 1975
  • Penrose L.S. Fingerprint patterns and the sex chromosomes. Lancet 1967; 1: 298–300
  • Penrose L.S., Loesch D. A study of dermal ridge-width in the second (palmar) interdigital area with special reference to aneuploid states. Journal of Mental Deficiency Research 1967; 11: 36–42
  • Pfeiffer R., Kiera W. Dermatoglyphen bei Turner-syndrome. Acta Genetica Medicae et Gemellolgiae 1968; 27: 507–522
  • Polani P.E., Polani N. Dermatoglyphics in the testicular feminization syndrome. Annals of Human Biology 1979; 6: 417–430
  • Reed T., Reichmann A., Palmar C. Dermatoglyphic differences between 45, X and other chromosomal abnormalities of Turner syndrome. Human Genetics 1977; 36: 13–23
  • Roberts D.F. Dermatoglyphics and human genetics. Dermatoglyphics — 50 Years later, Wertelecki W., Plato C. Alan R. Liss, New York 1979; 475–494, In
  • Saldana-Garcia P. A dermatoglyphic study of sixty-four XYY males. Annals of Human Genetics 1973; 37: 107–116
  • Saldana-Garcia P. Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy. Journal of Medical Genetics 1975; 12: 185–191
  • Stewart D., Bailey J., Netley C., Rovet J., Park E., Cripps M., Curtis J. Growth and development of children with X and Y chromosome aneuploidy from infancy to pubertal age: The Toronto study. Children with Sex Chromosome Aneuploidy: Follow-up Studies, Stewart D.A. Alan R. Liss, New York 1982; 99–154, In

Appendix: Sources of data

  • Alter M., Gorlin R., Yunis J., Peagler F., Bruhl H. Dermatoglyphics in XXYY Kline-felter's Syndrome. American Journal of Human Genetics 1966; 18: 507–513
  • Atkins L., Book J., Gustavson K.-H., Hausson O., Hyelm M. A case of XXXXY sex chromosome anomaly with autoradiographic studies. Cytogenetics 1966; 30: 1–6
  • Blackston R., Chen A. A case of 48, XXXX female with normal intelligence. Journal of Medical Genetics 1972; 9: 230–232
  • Bockzkowski K. Eunuchoidal female with 47, XYY karyotype. Annales de Genetique 1969; 12: 204–207
  • Cagno L. di, Franceschini P. Feeblemindedness and XXXX karyotype. Journal of Mental Deficiency Research 1968; 12: 226–236
  • Emberger J., Wagner A., Bonnet H. Congenital cardiac disease and 47, XYY karyotype: Study of Y chromosome replication. Annales de Genetique 1970; 13: 259–262
  • Farquhar H., Walker S. An XXXXY chromosome abnormality. Annals of Human Genetics 1964; 28: 11–19
  • Fraccaro M., Klinger H., Schutt W. A male with XXXXY sex chromosomes. Cytogenetics 1962; I: 52–52
  • Garcia H., Borgaonkar D., Richardson F. XXYY syndrome in a prepubertal male. Johns Hopkins Medical Journal 1967; 121: 31–37
  • Gilgenkrantz S., Gilliat J., Vautrin D. Syndrome 47, XXYY 13–14. Annales de Genetique 1970; 13: 201–206
  • Grouchy J. de, Brissaud H., Richardet J., Repesse G., Sanger R., Race R., Salmon Ch., Salmon D. Syndrome 48, XXXX chez une enfant de six ans transmission anormale du groupe Xg. Annales de Genetique 1968; 11: 120–124
  • Herbenval R., Gilgenkrantz S., Guerci O., Thibaut G. Syndrome de klinefelter a formula XXYY. La Presse Medicale 1965; 73: 2987–2998
  • Holt S. The Genetics of Dermal Ridges. Charles C. Thomas, Springfield 1968
  • Holt S., Lindsten J. Dermatoglyphic anomalies in Turner's Syndrome. Annals of Human Genetics 1964; 28: 87–100
  • Hreckzo T. The dermatoglyphics of a Toronto sample of children with XXY, XXYY, and XXX aneuploidies. American Journal of Physical Anthropology 1980; 52: 33–42
  • Hunter H. Finger and palm prints in chromatin positive males. Journal of Medical Genetics 1968; 5: 112–117
  • Insley J., Rushton D., Jones H. An intersexual infant with an extra chromosome. Annales de Genetique 1968; 11: 88–94
  • Jancar J. Mentally defective males with XXXXY chromosomes. Proceedings of the International Congress on the Scientific Study of Mental Retardation (Kobenhavn) 1964; 1: 179–195
  • Joseph M., Anders J., Taylor A. A boy with XXXXY sex chromosomes. Journal of Medical Genetics 1964; 1: 95–100
  • Koehn G., Winter J., Mellman W. Trisomy X in three children. Journal of Pediatrics 1968; 72: 248–252
  • Le Jeune J., Abonyi D. 48,XXXX syndrome in a fourteen year old girl. Annales de Genetique 1968; 11: 117–119
  • Lejeune J., Abonyi D., Berger R. Trisomy 18 and 47,XXX syndrome in the same sibship. Annales de Genetique 1969; 12: 59–61
  • Mavalwala J., Parker C., Melnyk J. Dermatoglyphics of the XYY syndrome. American Journal of Physical Anthropology 1969; 30: 209–214
  • Muller J.-M., Jalbert P., Cordonnier D. Syndrome de Klinefelter. Caryotype XXYY etude des dermatoglyphes. Annales Biologique Clinique 1967; 25: 207–214
  • Parker C., Mavalwala J., Melnyk J., Fish C. The 48,XXYY syndrome. American Journal of Medicine 1970; 48: 777–781
  • Parker C., Mavalwala J., Weise P., Kock R., Hatashita A., Cibilick S. The 47,XYY syndrome in a boy with behavior problems and mental retardation. American Journal of Mental Deficiency 1970; 74: 660–665
  • Pena S., Ray M., Douglas G. A 48, XXXX female. Journal of Medical Genetics 1973; 10: 211–215
  • Pfeiffer R., Kiera W. Dermatoglyphen bei Turner-Syndrom. Acta Genetica et Medicae Gemellologiae 1968; 27: 507–522
  • Quack B., Noel B., Durand Y. 47,XYY men. Annales de Genetique 1969; 12: 233–236
  • Reed T., Reichmann A., Palmar C. Dermatoglyphic differences between 45,X and other chromosomal abnormalities of Turner Syndrome. Human Genetics 1977; 36: 13–23
  • Robinson G., Miller J., Dill F., Kamburoff T. Klinefelter's Syndrome with the XXYY sex chromosome complex. Journal of Pediatrics 1964; 65: 226–232
  • Saldana-Garcia P. A dermatoglyphic study of sixty-four XYY males. Annals of Human Genetics 1973; 37: 107–116
  • Saldana-Garcia P. Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy. Journal of Medical Genetics 1975; 12: 185–192
  • Schlegel R., Aspellaga M., Neu R., Gardner L. Studies on a boy with XXYY chromosome constitution. Pediatrics 1965; 36: 113–119
  • Sokolowski J., Knaus A., Kleckowska A. Dermatoglyphics of two cases of X tetrasomy. American Journal of Human Genetics 1969; 21: 559–565
  • Telfer M., Richardson C., Helmken J. Divergent phenotypes among 48, XXXX and 47, XXX females. American Journal of Human Genetics 1970; 22: 326–335
  • Townes P., Ziegler N., Scherner A. An XXYY variant of the Klinefelter's syndrome in a prepubertal boy. Journal of Pediatrics 1965; 67: 410–414
  • Tsuboi T., Nelson J. Dermatoglyphic study of six patients with the XYY syndrome. Human Heredity 1969; 19: 299–306
  • Uchida I., Miller J., Soltan H. Dermatoglyphics associated with the XXYY chromosome complement. Journal of Pediatrics 1964; 69: 295–298
  • Vormittag W., Weninger M. XXXY Klinefelter-Syndrom. Humangenetik 1972; 15: 327–333

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