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[Heredity of congenital deficiencies in color vision]
scientific article published on 01 July 1972
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Europe PubMed Central
PubMed publication ID
4592447
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
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30 September 2019
review article
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title
[Heredity of congenital deficiencies in color vision]
(English)
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Europe PubMed Central
PubMed publication ID
4592447
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
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30 September 2019
author name string
J François
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1
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PubMed publication ID
4592447
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30 September 2019
S De Bie
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2
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PubMed publication ID
4592447
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G Verriest
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3
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PubMed publication ID
4592447
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30 September 2019
M T Matton
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4
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PubMed publication ID
4592447
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publication date
1 July 1972
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Europe PubMed Central
PubMed publication ID
4592447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 September 2019
published in
Acta geneticae medicae et gemellologiae
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Europe PubMed Central
PubMed publication ID
4592447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
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30 September 2019
volume
21
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Europe PubMed Central
PubMed publication ID
4592447
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
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30 September 2019
issue
3
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Europe PubMed Central
PubMed publication ID
4592447
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 September 2019
page(s)
233-256
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Europe PubMed Central
PubMed publication ID
4592447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
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30 September 2019
cites work
A case of unilateral deuteranopia
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7 January 2021
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On congenital tritanomaly
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7 January 2021
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Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia
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7 January 2021
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Color blindness among Korean students
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https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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Linkage scores and corrections in simple two- and three-generation families
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Crossref
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7 January 2021
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A sign of manifest heterozygosity in carriers of color deficiency
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Crossref
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https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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Mitotic separation of two human X-linked genes in man--mouse somatic cell hybrids
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7 January 2021
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Colour blindness and the Duchenne-type muscular dystrophy
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Crossref
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7 January 2021
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THE X-LINKED BLOOD GROUP SYSTEM XG.
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7 January 2021
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Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes
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Crossref
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7 January 2021
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A pedigree suggesting the inheritance of yellow-blue anomaly
1 reference
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7 January 2021
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Further studies on acquired deficiency of color discrimination
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Crossref
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7 January 2021
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Total achromatopsia in two brothers
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7 January 2021
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Red-Light Thresholds in Heterozygote Carriers of Protanopia: Genetic Implications
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7 January 2021
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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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7 January 2021
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Data for X-mapping calculations, Israeli families tested for Xg, g-6-pd and for colour vision
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7 January 2021
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Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's Disease
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7 January 2021
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Clinical study of colour vision
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Crossref
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7 January 2021
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PI-1 CONE MONOCHROMATISM.
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7 January 2021
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Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis
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7 January 2021
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inferred from DOI database lookup
Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome
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Crossref
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7 January 2021
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THE INHERITANCE OF CONGENITAL TRITANOPIA WITH THE REPORT OF AN EXTENSIVE PEDIGREE
1 reference
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reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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inferred from DOI database lookup
COLOR-VISION DEFECTS IN AMERICAN SCHOOL CHILDREN
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage relationships of the angiokeratoma (Fabry) locus
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Crossref
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https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
Combined forms of congenital colour defects; a pedigree with atypical total colour blindness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
The enigma of typical total monochromacy
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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inferred from DOI database lookup
The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker
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https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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inferred from DOI database lookup
Gene action in the X-chromosome of the mouse (Mus musculus L.)
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7 January 2021
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inferred from DOI database lookup
Linkage studies in X-linked retinitis pigmentosa
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reference URL
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7 January 2021
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inferred from DOI database lookup
The Linkage between the Genes for Colour-Blindness and Haemophilia in Man
1 reference
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reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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LYONISATION OF THE X CHROMOSOME
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
Human phosphoglycerate kinase and inactivation of the X chromosome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
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Colour vision in blue-cone 'monochromacy'.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
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DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
The linkage relation of Xg to g-6-pd in Israelis: the evidence of a second series of families
1 reference
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Crossref
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7 January 2021
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Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis
1 reference
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7 January 2021
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Linkage between Deficiency of Glucose-6-phosphate Dehydrogenase and Colour-blindness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical Achromatopia of Sex-Linked Recessive Inheritance*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Directed Genetic Change Model for X Chromosome Inactivation in Eutherian Mammals
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
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7 January 2021
based on heuristic
inferred from DOI database lookup
Spectral sensitivity in color-defective subjects and heterozygous carriers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of tritanopy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A branched-pathway schema for the color-vision system and some of the evidence for it
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Colour vision deficiency in one of two presumably monozy?otic twins with secondary amenorrhoea
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rod and cone receptor mechanisms in typical and atypical congenital achromatopsia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The familial distribution of congenital tritanopia, with some remarks on some similar conditions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Xg Locus : Failure to detect Inactivation in Females with Chronic Myelocytic Leukaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The incidence of red-green color deficiency in New Zealand's Maoris and "Islanders"
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ugandan colorblinds revisited
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Presumptive iso-chromosomes for the long arm of X in man. Analysis of five families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population differences in red and green color vision deficiency: a review, and a query on selection relaxation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RECOMBINATION BETWEEN PROTAN AND DEUTAN GENES; DATA ON THEIR RELATIVE POSITONS IN RESPECT OF THE G6PD LOCUS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Anomaloscopic Diagnoses of Red-Green Blindness Among Thais and Chinese
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Colour Vision of Heterozygotes for Sex-linked Red-Green Defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE X-LINKED RECESSIVE INHERITANCE OF ATYPICAL MONOCHROMATISM.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective color vision and its inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Red/green color blindness in the Niger delta
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The characteristics of tritanopia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transitory "positive" selection for colorblindness?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300010957
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S1120962300010957
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4592447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 September 2019
PubMed publication ID
4592447
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4592447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4592447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
30 September 2019
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