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4. Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes. Nucaro AL; Rossino R; Pruna D; Rassu S; Cianchetti C; Cao A; Moi P Prenat Diagn; 2006 May; 26(5):418-9. PubMed ID: 16532523 [TBL] [Abstract][Full Text] [Related]
5. De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches. Malvestiti F; De Toffol S; Grimi B; Chinetti S; Marcato L; Agrati C; Di Meco AM; Frascoli G; Trotta A; Malvestiti B; Ruggeri A; Dulcetti F; Maggi F; Simoni G; Grati FR Prenat Diagn; 2014 May; 34(5):460-8. PubMed ID: 24436202 [TBL] [Abstract][Full Text] [Related]
6. Cytogenetic analysis of chorionic villi for prenatal diagnosis: an ACC collaborative study of U.K. data. Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis. Prenat Diagn; 1994 May; 14(5):363-79. PubMed ID: 8084857 [TBL] [Abstract][Full Text] [Related]
7. Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH. Gole LA; Biswas A Prenat Diagn; 2005 Jan; 25(1):73-8. PubMed ID: 15662692 [TBL] [Abstract][Full Text] [Related]
8. Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study. Hu S; Kong X Taiwan J Obstet Gynecol; 2023 Jan; 62(1):94-100. PubMed ID: 36720559 [TBL] [Abstract][Full Text] [Related]
9. A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity. Reddy KS; Aradhya S; Meck J; Tiller G; Abboy S; Bass H Genet Med; 2013 Jan; 15(1):3-13. PubMed ID: 22935720 [TBL] [Abstract][Full Text] [Related]
10. Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes. Liehr T; Klein E; Mrasek K; Kosyakova N; Guilherme RS; Aust N; Venner C; Weise A; Hamid AB Cytogenet Genome Res; 2013; 139(3):158-63. PubMed ID: 23295254 [TBL] [Abstract][Full Text] [Related]
11. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH). Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777 [TBL] [Abstract][Full Text] [Related]
12. The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey. Karaman B; Aytan M; Yilmaz K; Toksoy G; Onal EP; Ghanbari A; Engur A; Kayserili H; Yuksel-Apak M; Basaran S Eur J Med Genet; 2006; 49(3):207-14. PubMed ID: 16762822 [TBL] [Abstract][Full Text] [Related]
13. Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Haddad BR; Schröck E; Meck J; Cowan J; Young H; Ferguson-Smith MA; du Manoir S; Ried T Hum Genet; 1998 Nov; 103(5):619-25. PubMed ID: 9860306 [TBL] [Abstract][Full Text] [Related]
14. Chromosomal mosaicism in amniotic cell culture. A diagnostic Dilemma. Kohn G; Mennuti MT; Kaback M; Schwartz RM; Chemke J; Goldman B; Mellman WJ Isr J Med Sci; 1975 May; 11(5):476-81. PubMed ID: 1158661 [TBL] [Abstract][Full Text] [Related]
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18. Five cases of prenatally diagnosed sex chromosome mosaicism. Nocera G; Dalpra' L; Tibiletti MG; Buscaglia M Prenat Diagn; 1985; 5(3):169-74. PubMed ID: 4022940 [TBL] [Abstract][Full Text] [Related]
19. The role of cordocentesis in assessment of mosaicism found in amniotic fluid cell culture. Shalev E; Zalel Y; Weiner E; Cohen H; Shneur Y Acta Obstet Gynecol Scand; 1994 Feb; 73(2):119-22. PubMed ID: 8116349 [TBL] [Abstract][Full Text] [Related]