(Q40676622)

22 September 2017

title

On the incidence of unilateral and bilateral colour blindness in heterozygous females (English)

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22 September 2017

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K Feig

1

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22 September 2017

H H Ropers

series ordinal

2

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22 September 2017

publication date

1 April 1978

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22 September 2017

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22 September 2017

volume

41

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22 September 2017

issue

3

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22 September 2017

page(s)

313-323

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Numerology of development.

22 September 2017

cites work

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Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia

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Preferential expression of the maternally derived X chromosome in the mouse yolk sac

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X-chromosome inactivation and selection in somatic cells

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Cell lineage in retinal development of mice studied in experimental chimaeras

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Variable composition of X chromosomal mosaics: Due to asynchronous cell division during early embryogenesis?

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Time of X Chromosome Inactivation in Retinal Melanocytes of the Mouse

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Colour Vision of Heterozygotes for Sex-linked Red-Green Defects

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X-chromosome inactivation and developmental patterns in mammals

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Quantitative diagnosis of defective color vision. A comparative evaluation of the Ishihara test, the Farnsworth dichotomous test and the Hardy-Rand-Rittler polychromatic plates

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[Studies on genetic carrier of color deficiency. 3. The result of color discrimination test.]

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A HUE DISCRIMINATION DEFECT IN SO-CALLED NORMAL CARRIERS OF COLOR VISION DEFECTS

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A sign of manifest heterozygosity in carriers of color deficiency

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Random inactivities of the X chromosome in intermediate X-linked retinitis pigmentosa. Two hypotheses.

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Spectral sensitivity in color-defective subjects and heterozygous carriers

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Variability and consistency in the manifestation of red-green colour vision defects

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The manifesting carrier in Duchenne muscular dystrophy

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Mammalian X-chromosome inactivation

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Data concerning colour vision deficiencies amongst 29,985 young Greeks

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Color perceptions of deuteranopic and protanopic observers

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Examination of color sense in practice

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COLOR-VISION DEFECTS IN AMERICAN SCHOOL CHILDREN

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The X chromosome and the eye. The implications of recent microbiological models for clinical ophthalmology

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Incidence of known and unknown colour vision defects. A study of 6526 secondary school pupils in Amsterdam

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STUDIES ON GENETIC CARRIERS OF COLOR DEFICIENCIES. 4. RESULTS OF A SATURATION DISCRIMINATION TEST

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[Studies on the genetic carrier of color deficiency.]

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GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE

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X chromosome inactivation mosaicism in the mouse

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The Frequency of Colour Blindness in the Newars of Nepal Valley

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Some heterozygous manifestations of colour blindness

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Color perception changes with age: test results by P-N anomaloscope

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Evidence for reduced colour vision in carriers of congenital colour vision deficiencies (author's transl)

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12 December 2020

Some visual functions of a unilaterally color-blind person. I. Critical fusion frequency in various spectral regions

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Gene action in the X-chromosome of the mouse (Mus musculus L.)

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Genetics of protan and deutan color-vision anomalies: an instructive family

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Sex Differences in Colour Vision

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12 December 2020

Unilateral colour vision disturbance. A family study

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12 December 2020

The colour vision characteristics of an observer with unilateral defective colour vision: Results and analysis

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THE SPECTRAL LUMINOSITY CURVES FOR A DICHROMATIC EYE AND A NORMAL EYE IN THE SAME PERSON.

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Sex-linked ocular albinism displaying typical fundus changes in the female heterozygote

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12 December 2020

Control of chromosome inactivation

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12 December 2020

Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).

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12 December 2020

Color discrimination in heterozygotes

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12 December 2020

Identifiers

DOI

10.1007/BF00284765

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Dimensions Publication ID

22 September 2017

1002265881

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