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6. Natural history of mosaic trisomy 14 syndrome. Fujimoto A, Allanson J, Crowe CA, Lipson MH, Johnson VP. Am J Med Genet; 1992 Sep 15; 44(2):189-96. PubMed ID: 1456290 [Abstract] [Full Text] [Related]
7. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance. Dallaire L. J Med Genet; 1969 Jun 15; 6(2):113-20. PubMed ID: 4389828 [No Abstract] [Full Text] [Related]
8. Tetrasomy 9p confirmed by GALT. Balestrazzi P, Croci G, Frassi C, Franchi F, Giovannelli G. J Med Genet; 1983 Oct 15; 20(5):396-9. PubMed ID: 6644773 [Abstract] [Full Text] [Related]
9. Partial trisomy 10q: a recognizable syndrome. Klep-de Pater JM, Bijlsma JB, de France HF, Leschot NJ, Duijndam-van den Berge M, van Hemel JO. Hum Genet; 1979 Jan 19; 46(1):29-40. PubMed ID: 429004 [Abstract] [Full Text] [Related]
14. [Trisomy 10 p. A previously reported case explained by binding]. Turleau C, Doussau de Bazignan M, Roubin M, de Grouchy J. Ann Genet; 1976 Mar 19; 19(1):61-4. PubMed ID: 1084125 [Abstract] [Full Text] [Related]