The genetics of tritan disturbances

Author:

Went L. N.,Pronk N.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Bell J (1926) Treasury of human inheritance, vol 2, part II. Cambridge University Press, London, pp 128?268

2. Birch-Cox J (1976) Design of diagnostic test for congenital and acquired colour vision defects. In: Verriest G (ed) Colour vision deficiencies III. Karger, Basel, pp 196?201

3. de Vries-de Mol EC, Went LN, van Norren D, Pols LCW (1978) Increment spectral sensitivity of hemizygotes and heterozygotes for different classes of colour vision. In: Verriest G (ed) Colour vision deficiencies IV. Karger, Basel, pp 224?228

4. de Vries-de Mol EC, Went LN (1978) Frequencies of different types of colour vision. Hum Hered 28:301?316

5. Henry GH, Cole BL, Nathan J (1964) The inheritance of congenital tritanopia with the report of an extensive pedigree. Ann Hum Genet 27:219?231

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