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PMID: 4548443 Published · ppublish English Journal Article

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

Journal of medical genetics ·Vol. 11 ·No. 4 ·1974-12-00 ·Pages 321-7

Zatz M, Itskan SB, Sanger R, Frota-Pessoa O, Saldanha PH

Abstract

暂无摘要

MeSH Terms
Blood Group Antigens Chromosome Mapping Color Vision Defects/genetics Creatine Kinase/blood Female Genetic Linkage Genetic Variation Glucosephosphate Dehydrogenase/blood Humans Male Muscular Dystrophies/genetics Pedigree Probability Recombination, Genetic Sex Chromosomes
Chemicals
Blood Group Antigens Glucosephosphate Dehydrogenase Creatine Kinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Zatz M
Itskan S B
Sanger R
Frota-Pessoa O
Saldanha P H
References (14)
14 references, click to expand
  1. A comparison of the two-generation and three-generation methods of estimating linkage values on the X chromosome in man with special reference to the loci determining the Xg blood group and glucose-6-phosphate dehydrogenase deficiency.
    Am J Hum Genet. 1968 Nov;20(6):534-48 PMID: 5703689
  2. Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.
    Ann Hum Genet. 1962 Nov;26:107-22 PMID: 13985567
  3. GLUCOSE-6-PHOSPHATE DEHYDROGENASE, COLOUR VISION AND XG BLOOD GROUPS IN GREECE: LINKAGE AND POPULATION DATA.
    Ann Hum Genet. 1964 Jun;27:395-403 PMID: 14175203
  4. Colour blindness and the Duchenne-type muscular dystrophy.
    Ann Hum Genet. 1956 Nov;21(2):155-8 PMID: 13373181
  5. [Genetics of myopathy].
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  6. Carrier detection in X-linked muscular dystrophy.
    J Genet Hum. 1969 Oct;17(3):497-510 PMID: 5387424
  7. Sequential tests for the detection of linkage.
    Am J Hum Genet. 1955 Sep;7(3):277-318 PMID: 13258560
  8. [A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].
    Humangenetik. 1966;3(1):17-29 PMID: 5986051
  9. The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus.
    Am J Hum Genet. 1965 Jul;17(4):325-42 PMID: 17948499
  10. The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.
    Ann Hum Genet. 1969 Jan;32(3):261-9 PMID: 5305175
  11. Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.
    J Med Genet. 1966 Jun;3(2):92-5 PMID: 5297734
  12. Linkage between deficiency of glucose-6-phosphate dehydrogenase and colour-blindness.
    Nature. 1961 Feb 25;189:686 PMID: 13681296
  13. Evidence for the absence of detectable linkage between the genes for Duchenne muscular dystrophy and the Xg blood group.
    Am J Hum Genet. 1963 Sep;15:292-7 PMID: 14021522
  14. Distribution and heredity of erythrocyte G6PD activity and electrophoretic variants among different racial groups at São Paulo, Brazil.
    J Med Genet. 1969 Mar;6(1):48-54 PMID: 5771222
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.11.4.321
Published
1974-12-00
Pages
321-7
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1013198
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.11.4.321 PMC Full Text View journal details
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