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Journal Abstract Search
157 related items for PubMed ID: 6632718
1. [Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes]. Meisel-Stosiek M, Pfeiffer RA, Tietze HU. Klin Padiatr; 1983; 195(5):365-8. PubMed ID: 6632718 [Abstract] [Full Text] [Related]
2. [Down's syndrome with predominantly normal karyotype in lymphocyte culture but extensive G trisomy in fibroblast culture]. Haberlandt W, Wunderlich C. Arztl Forsch; 1972 Sep 10; 26(9):309-16. PubMed ID: 4262890 [No Abstract] [Full Text] [Related]
3. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype. Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G. Prenat Diagn; 2003 Feb 10; 23(2):128-33. PubMed ID: 12575019 [Abstract] [Full Text] [Related]
4. Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones. Miller K, Arslan-Kirchner A, Schulze B, Dudel-Neujahr A, Morlot M, Burck U, Gerresheim F. Ann Genet; 1997 Feb 10; 40(3):181-4. PubMed ID: 9401109 [Abstract] [Full Text] [Related]
5. Trisomy 8 syndrome. A report of 2 cases. Ioan D, Dumitriu L, Muşeţeanu P, Belengeanu V, Pop T, Maximilian C. Endocrinologie; 1986 Feb 10; 24(1):45-8. PubMed ID: 3961414 [Abstract] [Full Text] [Related]
6. Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome. de France HF, Beemer FA, Senders RC, Schaminée-Main SC. Clin Genet; 1985 Jan 10; 27(1):92-6. PubMed ID: 3978842 [Abstract] [Full Text] [Related]
9. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies. Oikawa K, Kajii T, Shimba H, Sasaki M. Ann Genet; 1969 Jun 10; 12(2):102-6. PubMed ID: 5308379 [No Abstract] [Full Text] [Related]
11. Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infant. Schofield B, Babu A, Punales-Morejon D, Popescu S, Leiter E, Franklin B, Penchaszadeh VB. Am J Med Genet; 1992 Sep 01; 44(1):7-10. PubMed ID: 1519655 [Abstract] [Full Text] [Related]
12. Trisomy 8: an international study of 70 patients. Riccardi VM. Birth Defects Orig Artic Ser; 1977 Sep 01; 13(3C):171-84. PubMed ID: 890109 [Abstract] [Full Text] [Related]
13. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)]. Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J. Ann Genet; 1979 Sep 01; 22(3):178-81. PubMed ID: 316677 [Abstract] [Full Text] [Related]
18. Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata. Wertelecki W, Breg WR, Graham JM, Iinuma K, Puck SM, Sergovich FR. Am J Med Genet; 1986 Mar 23; 23(3):739-49. PubMed ID: 3953673 [Abstract] [Full Text] [Related]
19. Trisomy 18 mosaicism in a mildly retarded boy with postnatal overgrowth. Plessis G, Le Treust M, Lemaire F, Maugard T, Cau D. Ann Genet; 1997 Mar 23; 40(4):235-7. PubMed ID: 9526621 [Abstract] [Full Text] [Related]
20. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18? Shashi V, Golden WL, von Kap-Herr C, Wilson WG. Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322 [Abstract] [Full Text] [Related] Page: [Next] [New Search]