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Journal Abstract Search
164 related items for PubMed ID: 7450754
1. Trisomy 8. Report of a mosaic human male with near-normal phenotype and normal IQ, ascertained through infertility. Chandley AC, Hargreave TB, Fletcher JM, Soos M, Axworthy D, Price WH. Hum Genet; 1980; 55(1):31-8. PubMed ID: 7450754 [Abstract] [Full Text] [Related]
3. Triple mosaicism with two autosomally unbalanced cell lines in a phenotypically normal oligospermic man. Shabtai F, Bichacho S, Halbrecht I. Acta Genet Med Gemellol (Roma); 1977; 26(2):177-80. PubMed ID: 596115 [Abstract] [Full Text] [Related]
5. Trisomy 18 mosaicism: clues to the diagnosis. Bass HN, Fox M, Wulfsberg E, Sparkes RS, Crandall BF. Clin Genet; 1982 Dec; 22(6):327-30. PubMed ID: 7160104 [Abstract] [Full Text] [Related]
6. A clinical and molecular study of mosaicism for trisomy 17. Shaffer LG, McCaskill C, Hersh JH, Greenberg F, Lupski JR. Hum Genet; 1996 Jan; 97(1):69-72. PubMed ID: 8557263 [Abstract] [Full Text] [Related]
7. Double autosomal/gonosomal mosaic aneuploidy: study of nondisjunction in two cases with trisomy of chromosome 8. DeBrasi D, Genardi M, D'Agostino A, Calvieri F, Tozzi C, Varrone S, Neri G. Hum Genet; 1995 May; 95(5):519-25. PubMed ID: 7759072 [Abstract] [Full Text] [Related]
8. Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome. Miró R, Templado C, Ponsá M, Serradell J, Marina S, Egozcue J. Hum Genet; 1980 Feb; 53(2):179-82. PubMed ID: 7358385 [Abstract] [Full Text] [Related]
9. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies. Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G. Eur J Hum Genet; 1999 Feb; 7(4):421-6. PubMed ID: 10352932 [Abstract] [Full Text] [Related]
10. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes. Crowe CA, Schwartz S, Black CJ, Jaswaney V. Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446 [Abstract] [Full Text] [Related]
11. Mosaic trisomy 15 and hemihypertrophy. Gérard-Blanluet M, Elbez A, Bazin A, Danan C, Verloes A, Janaud JC. Ann Genet; 2001 Sep 05; 44(3):143-8. PubMed ID: 11694227 [Abstract] [Full Text] [Related]
12. First report of mosaic trisomy 12 in a liveborn individual. Patil SR, Bosch EP, Hanson JW. Am J Med Genet; 1983 Mar 05; 14(3):453-60. PubMed ID: 6859097 [Abstract] [Full Text] [Related]
13. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability. Naoufal R, Legendre M, Couet D, Gilbert-Dussardier B, Kitzis A, Bilan F, Harbuz R. Eur J Med Genet; 2016 Sep 05; 59(9):483-7. PubMed ID: 27452446 [Abstract] [Full Text] [Related]
14. Phenotypic spectrum of mosaic trisomy 18: two new patients, a literature review, and counseling issues. Tucker ME, Garringer HJ, Weaver DD. Am J Med Genet A; 2007 Mar 01; 143A(5):505-17. PubMed ID: 17266111 [Abstract] [Full Text] [Related]
15. Mosaic trisomy 8 detected by fibroblasts cultured of skin. Giraldo G, Gómez AM, Mora L, Suarez-Obando F, Moreno O. Colomb Med (Cali); 2016 Jun 30; 47(2):100-4. PubMed ID: 27546932 [Abstract] [Full Text] [Related]
16. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature. Kaplan LC, Wayne A, Crowell S, Latt SA. Am J Med Genet; 1986 Apr 30; 23(4):925-30. PubMed ID: 3515939 [Abstract] [Full Text] [Related]