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 *

159 related articles for article (PubMed ID: 17710877)

  • 1. Abnormal first trimester screen in partial deletion of chromosome 6p21: a case-report.
    Hulsbergen MH; Van Calenbergh SG; Fryns JP
    Genet Couns; 2007; 18(2):243-5. PubMed ID: 17710877
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Intermediate interstitial deletion of chromosome 7q detected by first-trimester Down's syndrome screening.
    Cheong ML; Tsai MS; Cortes RA; Harrison MR
    Fetal Diagn Ther; 2008; 24(4):340-4. PubMed ID: 18841024
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of and midtrimester pathology with karyotype 46,XY,del(4)(q22q26). A case report.
    Koppitch FC; Ramahi A; Quereshi F; Budev H; Perrin E; Evans MI
    J Reprod Med; 1990 Feb; 35(2):182-6. PubMed ID: 2304042
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Fetal chromosomal abnormalities: antenatal screening and diagnosis.
    Anderson CL; Brown CE
    Am Fam Physician; 2009 Jan; 79(2):117-23. PubMed ID: 19178062
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First-trimester prenatal diagnosis of a familial subtelomeric translocation.
    Kilby MD; Brackley KJ; Walters JJ; Morton J; Roberts E; Davison EV
    Ultrasound Obstet Gynecol; 2001 Jun; 17(6):531-3. PubMed ID: 11422979
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Fetal cyclopia with deletion 46,XX,del (7) (q32-->qter), prenatal diagnosis and genetic counseling].
    Hauschild R; Beensen V; Schulze E; Gross W
    Zentralbl Gynakol; 1993; 115(7):336-8. PubMed ID: 8368034
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cerebro-fronto-facial syndrome (Dandy-Walker Variant and frontofacial dysmorphisms): report of the first case identified by increased nuchal translucency beyond 13(+6) weeks.
    Tonni G; Azzoni D; Ambrosetti F; de Felice C; Ventura A
    Congenit Anom (Kyoto); 2007 Jun; 47(2):68-71. PubMed ID: 17504390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. First- and second-trimester screening: detection of aneuploidies other than Down syndrome.
    Breathnach FM; Malone FD; Lambert-Messerlian G; Cuckle HS; Porter TF; Nyberg DA; Comstock CH; Saade GR; Berkowitz RL; Klugman S; Dugoff L; Craigo SD; Timor-Tritsch IE; Carr SR; Wolfe HM; Tripp T; Bianchi DW; D'Alton ME;
    Obstet Gynecol; 2007 Sep; 110(3):651-7. PubMed ID: 17766613
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
    Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial chromosome deletion: a new trisomy rescue mechanism?
    Vialard F; Molina-Gomes D; Quarello E; Leroy B; Ville Y; Selva J
    Fetal Diagn Ther; 2009; 25(1):111-4. PubMed ID: 19246929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [The prenatal detection of trisomy 13, 18, and 21: comparison of the advanced first trimester screening (AFS) with the first trimester screening according to Nicolaides].
    Hörmansdörfer C; Schmidt P; Hillemanns P; Scharf A
    Z Geburtshilfe Neonatol; 2007 Dec; 211(6):243-9. PubMed ID: 18176905
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.
    Aslan H; Karaman B; Yildirim G; Ceylan Y
    Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308
    [TBL] [Abstract][Full Text] [Related]  

  • 17. First-trimester and second-trimester screening at a community hospital: experience from the first year of implementation.
    Philipson EH; Callahan M; Jelovsek JE
    Obstet Gynecol; 2008 Aug; 112(2 Pt 1):218-22. PubMed ID: 18669714
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The utility of detailed first trimester ultrasound examination in abnormal fetal nuchal translucency.
    Bronshtein M; Zimmer EZ; Blazer S
    Prenat Diagn; 2008 Nov; 28(11):1037-41. PubMed ID: 18925580
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo 7q deletion with a positive maternal serum triple test screening.
    Park IY; Jo YS; Shin JC; Sung IK; Kim M
    J Obstet Gynaecol Res; 2008 Feb; 34(1):85-7. PubMed ID: 18226135
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal detection of cyclopia associated with interstitial deletion of 2p.
    Grundy HO; Niemeyer P; Rupani MK; Ward VF; Wassman ER
    Am J Med Genet; 1989 Oct; 34(2):268-70. PubMed ID: 2817010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.