BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 18765938)

  • 1. Prenatal diagnosis of a 4q33-4qter deletion in a fetus with hydrops.
    Russell Z; Kontopoulos EV; Quintero RA; DeBauche DM; Ranells JD
    Fetal Diagn Ther; 2008; 24(3):250-3. PubMed ID: 18765938
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA; Packman S; Loughman WD; Fineman RM; Zackai E; Patil SR; Emanual B; Bartley JA; Hanson JW
    Am J Med Genet; 1981; 8(1):73-89. PubMed ID: 7246608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K; Sriphaisal T; Krutvecho T; Ketupanya A; Vuthiwong C; Suwanasophon C; Noonai A
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():287-90. PubMed ID: 8629126
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter).
    Calabrese G; Giannotti A; Mingarelli R; Di Gilio MC; Piemontese MR; Palka G
    Clin Genet; 1997 Apr; 51(4):264-7. PubMed ID: 9184250
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.
    Faivre L; Morichon-Delvallez N; Viot G; Martinovic J; Pinson MP; Aubry JP; Raclin V; Edery P; Dumez Y; Munnich A; Vekemans M
    Prenat Diagn; 1999 Jan; 19(1):49-53. PubMed ID: 10073907
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
    Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The 4q-Syndrome.
    Strehle EM; Ahmed OA; Hameed M; Russell A
    Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Prenatal diagnosis of deletion of chromosome 6p presenting with hydrops fetalis.
    Suwanrath-Kengpol C; Limprasert P; Mitarnun W
    Prenat Diagn; 2004 Nov; 24(11):887-9. PubMed ID: 15565585
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mosaicism for terminal deletion of 4q.
    Utine GE; Aktas D
    Genet Couns; 2006; 17(2):205-9. PubMed ID: 16970039
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of mosaicism for 11q terminal deletion.
    Valduga M; Cannard VL; Philippe C; Romana S; Miton A; Droulle P; Foliguet B; Lecompte T; Jonveaux P
    Eur J Med Genet; 2007; 50(6):475-81. PubMed ID: 17761465
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Second-trimester diagnosis of mucopolysaccharidosis type IV a presenting as hydrops fetalis.
    Colmant C; Picone O; Froissart R; Labrune P; Senat MV
    Prenat Diagn; 2006 Aug; 26(8):750-2. PubMed ID: 16865740
    [No Abstract]   [Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M; Martinovic J; Sanlaville D; AttiƩ-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
    Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
    Sills ES; Burns MJ; Parker LD; Carroll LP; Kephart LL; Dyer CS; Papenhausen PR; Davis JG
    Orphanet J Rare Dis; 2007 Feb; 2():9. PubMed ID: 17295911
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
    Knegt AC; Li S; Engelen JJ; Bijlsma EK; Warburton PE
    Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.