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5. A family with three sibs carrying trisomy 21. Nuzzo F, Stefanini M, Simoni G, Larizza L, Mottura A, Reali E, Franceschini P. Ann Genet; 1975 Jun; 18(2):111-6. PubMed ID: 127545 [Abstract] [Full Text] [Related]
6. Twins, probably monozygotic, displaying Down's syndrome, physical and functional mirror-imaging, and discordance for congenital heart disease. Telfer MA, Baker D, Bergman M. Am J Ment Defic; 1972 Jan; 76(4):391-6. PubMed ID: 4258447 [No Abstract] [Full Text] [Related]
12. Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome. Weiss L, Wolf CB. Am J Dis Child; 1968 Dec; 116(6):609-14. PubMed ID: 4235163 [No Abstract] [Full Text] [Related]
13. A mother with Down's syndrome and her chromosomally normal infant. Reiss JA, Lovrien EW, Hecht F. Ann Genet; 1971 Sep; 14(3):225-7. PubMed ID: 4255605 [No Abstract] [Full Text] [Related]
16. [Dermatoglyphics of the palms and fingers in Down's syndrome with partial trisomy of chromosome 21]. Gebala A, Jakliński A, Dobrzańska A, Iwaszkiewicz A, Grzeszyk C. Pol Tyg Lek; 1969 Jun 09; 24(23):867-70. PubMed ID: 4240984 [No Abstract] [Full Text] [Related]
18. Parental dermatoglyphics in Down's syndrome. A ten-year study. Priest JH, Verhulst C, Sirkin S. J Med Genet; 1973 Dec 09; 10(4):328-32. PubMed ID: 4272738 [Abstract] [Full Text] [Related]
19. [Cytogenetic and dermatoglyphic studies in Down's syndrome with G-G translocation]. Trebicka-Kwiatkowska B, Raczkiewicz B, Galińska I, Gasiorowski A. Pol Tyg Lek; 1973 Aug 06; 28(32):1220-2. PubMed ID: 4270748 [No Abstract] [Full Text] [Related]
20. [t(7q-; 21q-plus) and familial and trisomy 21]. Giraud F, Hartung M, Mattei JF, Mattie MG. Ann Genet; 1974 Mar 06; 17(1):49-53. PubMed ID: 4276449 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]