(Q35231983)

7 August 2017

title

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

1 reference

7 August 2017

Thuline HC

1

1 reference

7 August 2017

Hodgkin WE

series ordinal

2

1 reference

7 August 2017

Fraser GR

series ordinal

3

1 reference

7 August 2017

Motulsky AG

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 November 1969

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

21

1 reference

7 August 2017

issue

6

1 reference

7 August 2017

page(s)

581-592

1 reference

AN ANALYSIS OF SOME DATA ON THE LINKAGE BETWEEN XG AND COLORBLINDNESS IN MAN

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

X CHROMOSOME MAPPING OF GENES FOR RED-GREEN COLORBLINDNESS AND XG

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

RECOMBINATION BETWEEN PROTAN AND DEUTAN GENES; DATA ON THEIR RELATIVE POSITONS IN RESPECT OF THE G6PD LOCUS.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

Hereditary, X-linked, sideroachrestic anemia. The isolation of two erythrocyte populations differing in Xga blood type and porphyrin content

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

Estimation of the recombination fraction between the protan and deutan loci

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

Defective color vision and its inheritance

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

Hurler's syndrome. A genetic study in cell culture

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

THE RED-LIGHT ABSOLUTE THRESHOLD IN HETEROZYGOTE PROTAN CARRIERS. POSSIBLE GENETIC IMPLICATIONS.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706480

A newly defined X-linked trait in man with demonstration of the Lyon effect in carrier females

26 September 2018

1 reference

12 December 2020

Distance and Sequence of the Loci for Protan and Deutan Defects and for Glucose-6-Phosphate Dehydrogenase Deficiency

1 reference

12 December 2020

COLOR-VISION DEFECTS IN AMERICAN SCHOOL CHILDREN

1 reference

12 December 2020

AGAMMAGLOBULINEMIA: THE FUNDAMENTAL DEFECT

1 reference

12 December 2020

Red-Light Thresholds in Heterozygote Carriers of Protanopia: Genetic Implications

1 reference

12 December 2020

Identifiers

PMC publication ID

1706480

1 reference

7 August 2017

1 reference