BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 9885024)

  • 1. Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathy.
    Witters I; Van Buggenhout G; Moerman P; Fryns JP
    Prenat Diagn; 1998 Dec; 18(12):1304-7. PubMed ID: 9885024
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Sonographic detection of hygroma colli in the fetus].
    Friese K; Merz E
    Ultraschall Med; 1989 Feb; 10(1):25-8. PubMed ID: 2652289
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli.
    Schwanitz G; Zerres K; Gembruch U; Bald R; Hansmann M
    Hum Genet; 1989 Dec; 84(1):81-2. PubMed ID: 2606481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
    Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo translocation t(5;9)(q11.2;p22) associated with hydrops fetalis and cystic hygroma.
    Eisbrenner K; Steffensen TS; Whiteman VE; Gilbert-Barness E
    Fetal Pediatr Pathol; 2012 Apr; 31(2):39-42. PubMed ID: 22217146
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17.
    Schwanitz G; Zerres K; Niesen M; Haverkamp F; Schmid G
    Ann Genet; 1988; 31(3):186-9. PubMed ID: 3066282
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP; Wang LK; Chern SR; Wu PS; Ko K; Chen YN; Chen SW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
    Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
    Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cystic hygroma colli: perinatal outcome after prenatal diagnosis.
    Droste S; Hendricks SK; Von Alfrey H; Mack LA
    J Perinat Med; 1991; 19(6):449-54. PubMed ID: 1839996
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chorionic villus sampling after first trimester diagnosis of fetal cystic hygroma colli.
    Pons JC; Diallo AA; Eydoux P; Rais S; Doumerc S; Frydman R; Papiernik E
    Eur J Obstet Gynecol Reprod Biol; 1989 Nov; 33(2):141-6. PubMed ID: 2684696
    [TBL] [Abstract][Full Text] [Related]  

  • 15. De novo reciprocal translocation t(5;11)(q22;p15) associated with hydrops fetalis (reciprocal translocation and hydrops fetalis).
    Pala HG; Artunc-Ulkumen B; Uyar Y; Bal F; Baytur YB; Koyuncu FM
    Fetal Pediatr Pathol; 2015 Feb; 34(1):44-8. PubMed ID: 25289481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fetal cystic hygroma colli: antenatal diagnosis, significance, and management.
    Garden AS; Benzie RJ; Miskin M; Gardner HA
    Am J Obstet Gynecol; 1986 Feb; 154(2):221-5. PubMed ID: 3511710
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Comment on the case report "Hygroma colli--sonographic indications of fetal chromosome abnormality", by A. Yilmaztürk and F. Deppermann].
    Brühwiler B; Rabner M; Lüscher KP
    Zentralbl Gynakol; 1992; 114(9):474-5. PubMed ID: 1369752
    [No Abstract]   [Full Text] [Related]  

  • 18. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
    Burégio-Frota P; Valença L; Leal GF; Duarte AR; Bispo-Brito AV; Soares-Ventura EM; Marques-Salles TJ; Nogueira MT; Muniz MT; Silva ML; Hunstig F; Liehr T; Santos N
    Genet Mol Res; 2010 Apr; 9(2):780-4. PubMed ID: 20449811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct dysmorphic syndrome in a child with inverted distal 5q duplication.
    Fryns JP; Kleczkowska A; Borghgraef M; Raveschot J; Van den Berghe H
    Ann Genet; 1987; 30(3):186-8. PubMed ID: 3499858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
    Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.