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• W2052977897 abstract "HereditasVolume 57, Issue 3 p. 373-381 Open Access SECONDARY SEX RATIO IN FAMILIES WITH X-CHROMOSOMAL DISORDERS A. W. ERIKSSON, A. W. ERIKSSON SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorBIRGITTA VAINIO-MATTILA, BIRGITTA VAINIO-MATTILA SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorU. KRAUSE, U. KRAUSE SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorJ. FELLMAN, J. FELLMAN SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorH. FORSIUS, H. FORSIUS SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this author A. W. ERIKSSON, A. W. ERIKSSON SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorBIRGITTA VAINIO-MATTILA, BIRGITTA VAINIO-MATTILA SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorU. KRAUSE, U. KRAUSE SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorJ. FELLMAN, J. FELLMAN SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this authorH. FORSIUS, H. FORSIUS SAMFUNDET FOLKHÄLSAN, INSTITUTE OF HUMAN GENETICS, HELSINGFORS PORI CENTRAL HOSPITAL, EYE DEPARTMENT, AND UNIVERSITY EYE HOSPITAL, OULU, FINLANDSearch for more papers by this author First published: October 1967 https://doi.org/10.1111/j.1601-5223.1967.tb02122.xCitations: 1AboutPDF ToolsExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Literature cited Forsius, H., Vainio-Mattila, B. and Eriksson, A. W. 1962. X-linked hereditary retinoschisis. Brit. J. Ophthalmol. 46: 678– 681. Forsius, H., Eriksson, A. W. and Vainio-Mattila, B. 1963. Geschlechtsgebundene erbliche Retinoschisis in zwei Familien in Finnland. Klin. Mbl. Augenheilk. 143: 806– 816. Ikkala, E. 1960. Haemophilia. A study of its laboratory, clinical, genetic and social aspects based on known haemophiliacs in Finland. Diss., Helsinki. Scand. J. Clin. Lab. Invest. Vol. 12, Suppl. 45. Kang, S. and Cho, W. 1959. The sex ratio at birth of the Korean population. Eugen Quart. 6: 187– 195. Lehmann, W. 1966. Personal communication. Moor-Jankowski, J. K., Huser, H. J., Rosin, S., Truog, G., Schneeberger, Maria and Geiger, M. 1958. Haemophilia B. Genetische, klinische und gerinnerungs-physiologische Aspekte (Untersuchungen an einem weitverbreiteten Bluterstamm). — S. Karger, Basel . Novitski, E. and Kimball, A. W. 1958. Birth order, parental ages, and sex of offspring. Amer. J. Hum. Genet. 10: 268– 275. Ramgren, O. 1962. A clinical and medico-social study of Haemophilia in Sweden. — Diss. Sthlm. Acta Med. Scand. Suppl. 379. Citing Literature Volume57, Issue3October 1967Pages 373-381 ReferencesRelatedInformation" @default.
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• W2052977897 title "SECONDARY SEX RATIO IN FAMILIES WITH X-CHROMOSOMAL DISORDERS" @default.
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