These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

500 related articles for article (PubMed ID: 8821848)

  • 1. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
    Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
    Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
    Wallerstein R; Yu MT; Neu RL; Benn P; Lee Bowen C; Crandall B; Disteche C; Donahue R; Harrison B; Hershey D; Higgins RR; Jenkins LS; Jackson-Cook C; Keitges E; Khodr G; Lin CC; Luthardt FW; Meisner L; Mengden G; Patil SR; Rodriguez M; Sciorra LJ; Shaffer LG; Stetten G; Van Dyke DL; Wang H
    Prenat Diagn; 2000 Feb; 20(2):103-22. PubMed ID: 10694683
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatally diagnosed balanced chromosome rearrangements: eight years' experience.
    Peng HH; Chao AS; Wang TH; Chang YL; Chang SD
    J Reprod Med; 2006 Sep; 51(9):699-703. PubMed ID: 17039698
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
    Hsu LY; Yu MT; Neu RL; Van Dyke DL; Benn PA; Bradshaw CL; Shaffer LG; Higgins RR; Khodr GS; Morton CC; Wang H; Brothman AR; Chadwick D; Disteche CM; Jenkins LS; Kalousek DK; Pantzar TJ; Wyatt P
    Prenat Diagn; 1997 Mar; 17(3):201-42. PubMed ID: 9110367
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
    Daniel A; Hook EB; Wulf G
    Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome mosaicism in 6,000 amniocenteses.
    Wilson MG; Lin MS; Fujimoto A; Herbert W; Kaplan FM
    Am J Med Genet; 1989 Apr; 32(4):506-13. PubMed ID: 2773995
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA; Wolff DJ; Dickerman LH; Redline R; Conroy JM; Schwartz S
    Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP; Porter HJ; Young ID
    Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408
    [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. Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
    Leppig KA; Disteche CM
    Semin Reprod Med; 2001 Jun; 19(2):147-57. PubMed ID: 11480912
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
    Langlois S; Yong PJ; Yong SL; Barrett I; Kalousek DK; Miny P; Exeler R; Morris K; Robinson WP
    Prenat Diagn; 2006 Jun; 26(6):548-58. PubMed ID: 16683298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytogenetic results from the U.S. Collaborative Study on CVS.
    Ledbetter DH; Zachary JM; Simpson JL; Golbus MS; Pergament E; Jackson L; Mahoney MJ; Desnick RJ; Schulman J; Copeland KL
    Prenat Diagn; 1992 May; 12(5):317-45. PubMed ID: 1523201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases.
    Yaegashi N; Senoo M; Uehara S; Suzuki H; Maeda T; Fujimori K; Hirahara F; Yajima A
    J Hum Genet; 1998; 43(2):85-90. PubMed ID: 9621511
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC).
    Prenat Diagn; 1999 Jan; 19(1):29-35. PubMed ID: 10073903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of de novo X;autosome translocations.
    Abrams L; Cotter PD
    Clin Genet; 2004 May; 65(5):423-8. PubMed ID: 15099352
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three cases of mosaicism for balanced reciprocal translocations.
    Leegte B; Sikkema-Raddatz B; Hordijk R; Bouman K; van Essen T; Castedo S; de Jong B
    Am J Med Genet; 1998 Oct; 79(5):362-5. PubMed ID: 9779802
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases.
    Warburton D; Anyane-Yeboa K; Francke U
    Am J Med Genet; 1987 Jun; 27(2):275-83. PubMed ID: 3605213
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Mar; 49(1):62-8. PubMed ID: 20466295
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.