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5. Report of the Committee on the Genetic Constitution of the X Chromosome. Birth Defects Orig Artic Ser; 1975; 11(3):20-5. PubMed ID: 1081890 [No Abstract] [Full Text] [Related]
6. New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups. Zatz M; Itskan SB; Sanger R; Frota-Pessoa O; Saldanha PH J Med Genet; 1974 Dec; 11(4):321-7. PubMed ID: 4548443 [TBL] [Abstract][Full Text] [Related]
8. The linkage between Duchenne-type progressive muscular dystrophy and color blindness. Prot J; Laska M Pol Med J; 1970; 9(5):1207-11. PubMed ID: 5313771 [No Abstract] [Full Text] [Related]
9. Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness. Wu LZ; Zeng LH; Ma QY; Xie YJ; Chen YZ; Wu DZ Jpn J Ophthalmol; 1988; 32(2):236-45. PubMed ID: 3263528 [TBL] [Abstract][Full Text] [Related]
10. [Recent progress in the diagnosis and treatment of genetic diseases]. Koller PC Recenti Prog Med; 1976 Oct; 61(4):557-70. PubMed ID: 828969 [No Abstract] [Full Text] [Related]
11. Crossing-over in a pedigree containing haemophilic and colour-blind individuals. RIDDELL WJ Ann Eugen; 1946 Apr; 13():30-4. PubMed ID: 20982097 [No Abstract] [Full Text] [Related]
13. Some congenital defects of the nervous system. Bird AV S Afr Med J; 1967 Feb; 41(7):165-7. PubMed ID: 4225751 [No Abstract] [Full Text] [Related]
14. Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness. Skinner R; Smith C; Emery AE J Med Genet; 1974 Dec; 11(4):317-20. PubMed ID: 4548442 [TBL] [Abstract][Full Text] [Related]
15. Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating. Greig DN J Med Genet; 1977 Apr; 14(2):130-2. PubMed ID: 300790 [TBL] [Abstract][Full Text] [Related]
16. [Hemophilia and Duchenne de Boulogne myopathy. Genetics]. Battin J; Serville F Rev Prat; 1994 Sep; 44(14):1955-60. PubMed ID: 7939289 [No Abstract] [Full Text] [Related]
17. Normal and abnormal color-vision genes. Motulsky AG Am J Hum Genet; 1988 Mar; 42(3):405-7. PubMed ID: 3258123 [No Abstract] [Full Text] [Related]
18. The detection of carriers and the problem of heterogeneity in genetic counseling. Porter IH Birth Defects Orig Artic Ser; 1970 May; 6(1):23-5. PubMed ID: 4257329 [No Abstract] [Full Text] [Related]
19. Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis. Adam A; Ziprkowski L; Feinstein A; Sanger R; Tippett P; Gavin J; Race RR Ann Hum Genet; 1969 May; 32(4):323-32. PubMed ID: 5307230 [No Abstract] [Full Text] [Related]
20. [Enzyme genetics]. Gedda L; Del Porto G; Brenci G Quad Sclavo Diagn; 1971 Mar; 7(1):161-70. PubMed ID: 5155177 [No Abstract] [Full Text] [Related] [Next] [New Search]