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 *

212 related articles for article (PubMed ID: 17330228)

  • 21. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
    Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
    J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of an interstitial 12q chromosome deletion.
    Pérez Sánchez C; Ayensa F; Lloveras E; Zamora L; Cirigliano V; Pérez E; Plaja A
    Ann Genet; 2004; 47(2):177-9. PubMed ID: 15183750
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosis.
    Rodriguez-Revenga L; Badenas C; Madrigal I; Sánchez A; Soler A; Carrió A; Milà M
    Prenat Diagn; 2005 Jun; 25(6):448-50. PubMed ID: 15966059
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Chen LF; Wang W
    Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP; Su YN; Chen YY; Chern SR; Liu YP; Wu PC; Lee CC; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Post-zygotic origin of isochromosome 12p.
    de Ravel TJ; Keymolen K; van Assche E; Wittevronghel I; Moerman P; Salden I; Matthijs G; Fryns JP; Vermeesch JR
    Prenat Diagn; 2004 Dec; 24(12):984-8. PubMed ID: 15614858
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus.
    Bijlsma EK; Knegt AC; Bilardo CM; Goodman FR
    Prenat Diagn; 2005 Jan; 25(1):39-44. PubMed ID: 15662696
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
    Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH.
    Malvestiti F; De Toffol S; Chinetti S; Grimi B; Favero G; Borsatti A; Maggi F; Simoni G; Romana Grati F
    Prenat Diagn; 2010 Mar; 30(3):280-3. PubMed ID: 20049850
    [No Abstract]   [Full Text] [Related]  

  • 30. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
    López I; Bafalliu JA; Bernabé MC; García F; Costa M; Guillén-Navarro E
    Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interstitial deletion del(10)(q25.2q25.3 approximately 26.11)--case report and review of the literature.
    Kehrer-Sawatzki H; Daumiller E; Müller-Navia J; Kendziorra H; Rossier E; du Bois G; Barbi G
    Prenat Diagn; 2005 Oct; 25(10):954-9. PubMed ID: 16088867
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A retrospective and theoretical evaluation of rapid methods for detecting chromosome abnormalities and their implications on genetic counseling based on a series of 3868 CVS diagnoses.
    Soler A; Morales C; Badenas C; Rodríguez-Revenga L; Carrió A; Margarit E; Costa D; Borrell A; Goncé A; Milà M; Sánchez A
    Fetal Diagn Ther; 2008; 23(2):126-31. PubMed ID: 18046070
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
    Wu YC; Fang JS; Lee KF; Estipona J; Yang ML; Yuan CC
    Prenat Diagn; 2003 Feb; 23(2):124-7. PubMed ID: 12575018
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
    Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.
    Fischer W; Dermitzel A; Osmers R; Pruggmayer M
    Prenat Diagn; 2001 Jun; 21(6):481-3. PubMed ID: 11438954
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome.
    Satre V; Monnier N; Devillard F; Amblard F; Lunardi J
    Prenat Diagn; 2004 Nov; 24(11):913-7. PubMed ID: 15565644
    [TBL] [Abstract][Full Text] [Related]  

  • 37. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
    BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis by array-CGH.
    Rickman L; Fiegler H; Carter NP; Bobrow M
    Eur J Med Genet; 2005; 48(3):232-40. PubMed ID: 16179219
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal detection of a de novo Yqh-acrocentric translocation.
    Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
    Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
    [TBL] [Abstract][Full Text] [Related]  

  • 40. (Potential) false-negative diagnoses in chorionic villi and a review of the literature.
    van den Berg C; Van Opstal D; Polak-Knook J; Galjaard RJ
    Prenat Diagn; 2006 May; 26(5):401-8. PubMed ID: 16538702
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.