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 *

677 related articles for article (PubMed ID: 10521829)

  • 1. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature.
    Chen CP; Huang MC; Chern SR; Kuo YL; Chen YN; Wu PS; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2015 Jun; 54(3):297-302. PubMed ID: 26166345
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.
    Chen CP; Wang TH; Lin CC; Tsai FJ; Hsieh LJ; Wang W
    J Formos Med Assoc; 2008 Oct; 107(10):822-6. PubMed ID: 18926951
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations.
    Chuang L; Kuo PL; Yang HB; Chien CH; Chen PY; Chang CH; Chang FM
    Prenat Diagn; 2003 Feb; 23(2):134-7. PubMed ID: 12575020
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly.
    Chen CP; Liu FF; Jan SW; Lin CL; Lan CC
    Clin Genet; 1996 Nov; 50(5):321-6. PubMed ID: 9007318
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strong variable clinical presentation in 3 patients with 7q terminal deletion.
    Frints SG; Schrander-Stumpel CT; Schoenmakers EF; Engelen JJ; Reekers AB; Van den Neucker AM; Smeets E; Devlieger H; Fryns JP
    Genet Couns; 1998; 9(1):5-14. PubMed ID: 9555580
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly.
    Ginocchio VM; De Brasi D; Genesio R; Ciccone R; Gimelli S; Fimiani F; de Berardinis T; Nitsch L; Banfi S; Magli A; Della Casa R
    Eur J Med Genet; 2008; 51(6):658-65. PubMed ID: 18762283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
    Chen CP; Liu FF; Jan SW; Lin SP; Lan CC
    Prenat Diagn; 1996 Mar; 16(3):270-5. PubMed ID: 8710784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
    Chen CP; Chern SR; Hsu CY; Lee CC; Lee MS; Wang W
    Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
    [No Abstract]   [Full Text] [Related]  

  • 14. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
    Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
    Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.
    Le Caignec C; Winer N; Boceno M; Delnatte C; Podevin G; Liet JM; Quere MP; Joubert M; Rival JM
    Prenat Diagn; 2003 Dec; 23(12):981-4. PubMed ID: 14663834
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 4 in a fetus with cyclopia and other anomalies.
    Van Allen MI; Ritchie S; Toi A; Fong K; Winsor E
    Am J Med Genet; 1993 Apr; 46(2):193-7. PubMed ID: 8484409
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
    Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract]   [Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
    Chen CP; Hung FY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):288-92. PubMed ID: 27125417
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP; Lin SP; Su YN; Tsai FJ; Wu PC; Town DD; Chen LF; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.