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Journal Abstract Search
112 related items for PubMed ID: 4549004
1. An informative large pedigree with four compound hemizygotes of three combinations of deutan and protan genes. Arias S, Rodríguez A. Acta Cient Venez; 1973; 24(2):44-52. PubMed ID: 4549004 [No Abstract] [Full Text] [Related]
2. New families, one with two recombinants for estimation of recombination between the deutan and protan loci. Arias S, Rodríguez A. Humangenetik; 1972; 14(4):264-8. PubMed ID: 4538150 [No Abstract] [Full Text] [Related]
3. Non-allelic compounds of protan and deutan deficiencies. Jaeger W, Lauer HJ. Mod Probl Ophthalmol; 1976; 17():121-30. PubMed ID: 1085856 [No Abstract] [Full Text] [Related]
6. [Intrafamilial association of complete and incomplete congenital achromatopsia with amblyopia and atypical (without amblyopia) of dominant autosomal transmission]. Ponte F, Scialfa A. Ann Ottalmol Clin Ocul; 1968 Jun; 94(6):608-32. PubMed ID: 5312373 [No Abstract] [Full Text] [Related]
17. Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals. Michaelides M, Johnson S, Simunovic MP, Bradshaw K, Holder G, Mollon JD, Moore AT, Hunt DM. Eye (Lond); 2005 Jan; 19(1):2-10. PubMed ID: 15094734 [Abstract] [Full Text] [Related]
19. Family history studies: V. The genetics of mania. Reich T, Clayton PJ, Winokur G. Am J Psychiatry; 1969 Apr; 125(10):1358-69. PubMed ID: 5304735 [No Abstract] [Full Text] [Related]
20. [Dominant transmitted optic atrophy combined with red-green-blindness in the sense of an acquired deutero disorder]. Früh D, Lauer HJ. Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972 Apr; 71():517-22. PubMed ID: 4542560 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]