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 *

142 related articles for article (PubMed ID: 8415421)

  • 1. A rare inherited euchromatic heteromorphism on chromosome 1.
    Zaslav AL; Blumenthal D; Fox JE; Thomson KA; Segraves R; Weinstein ME
    Prenat Diagn; 1993 Jul; 13(7):569-73. PubMed ID: 8415421
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Extra euchromatic band in the qh region of chromosome 9.
    von Beust G; Bink K
    Fetal Diagn Ther; 1999; 14(1):35-7. PubMed ID: 10072648
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis in the presence of an extra small chromosome in amniotic cell culture.
    Chen H; Harris J
    Ann Genet; 1980; 23(2):97-9. PubMed ID: 6967293
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Euchromatic heteromorphism or duplication without phenotypic effect?
    Barber JC
    Prenat Diagn; 1994 Apr; 14(4):323-4. PubMed ID: 8066046
    [No Abstract]   [Full Text] [Related]  

  • 5. Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4.
    Zaslav AL; Pierno G; Fougner A; Jacob J; Shikora G; Kazi R; Blumenthal D; Alexander F; Fox JE
    Am J Med Genet A; 2004 May; 126A(4):420-2. PubMed ID: 15098241
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of chromosome microarray analysis for prenatal diagnosis of a fetus with partial duplication of 1p and uniparental disomy of chromosome 6].
    Zhu R; Zhu X; Wang Y; Li J; Ru T; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):819-22. PubMed ID: 26663056
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Euchromatic variants of 8q21.2 in twins.
    Song XH; Hsu HK; Su MT; Chang TS; Su PY; Chen M; Kuo PL
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):227-229. PubMed ID: 28420513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Euchromatic variant 16p+. Implications in prenatal diagnosis.
    López Pajares I; Villa O; Salido M; Mori MA; Gonzalez A; Lapunzina P; De Torres ML; Vallcorba I; Palomares M; Fernández L; Delicado A
    Prenat Diagn; 2006 Jun; 26(6):535-8. PubMed ID: 16634122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency: A case report and literature review.
    Sun M; Yue F; Yu Y; Li L; Jiang Y; Zhang H; Liu R
    Medicine (Baltimore); 2020 Oct; 99(40):e22496. PubMed ID: 33019446
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis.
    Martin AO; Northrup H; Ledbetter DH; Trask B; van den Engh G; Le Beau MM; Beaudet AL; Gray JW; Sekhon G; Krassikoff N
    Am J Med Genet; 1988 Nov; 31(3):643-54. PubMed ID: 3228143
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
    Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR
    J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Constitutional heteromorphism of 9q13 --> q21 in a patient with chronic myelogenous leukemia.
    Surana RB; Rafi SK; Christopher KL; Reid TJ; Weiss RB
    Clin Genet; 1995 Jun; 47(6):321-3. PubMed ID: 7554367
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Extreme variant of enlarged heterochromatin region on chromosome 9Q in a normal child and multiple family members.
    Steffensen TS; Gilbert-Barness E; Sandstrom M; Bell JR; Bryan J; Sutcliffe MJ
    Fetal Pediatr Pathol; 2009; 28(6):247-52. PubMed ID: 19842879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two extra euchromatic bands in the qh region of chromosome 9.
    Ozkinay F; Ercal D; Ozkinay C; Onay H; Bora E; Erler A
    Genet Couns; 2005; 16(1):45-8. PubMed ID: 15844778
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling.
    Fineman RM; Issa B; Weinblatt V
    Am J Med Genet; 1989 Apr; 32(4):498-9. PubMed ID: 2773992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Extra G positive band on the long arm of chromosome 9.
    Knight LA; Soon GM; Tan M
    J Med Genet; 1993 Jul; 30(7):613. PubMed ID: 8411040
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication of euchromatin without phenotypic effects: a variant of chromosome 16.
    Bryke CR; Breg WR; Potluri VR; Yang-Feng TL
    Am J Med Genet; 1990 May; 36(1):43-4. PubMed ID: 2333906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.