BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 16258951)

  • 1. Prenatal forehead edema in 4p- deletion: the 'Greek warrior helmet' profile revisited.
    Levaillant JM; Touboul C; Sinico M; Vergnaud A; Serero S; Druart L; Blondeau JR; Abd Alsamad I; Haddad B; Gérard-Blanluet M
    Prenat Diagn; 2005 Dec; 25(12):1150-5. PubMed ID: 16258951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of de novo pure partial monosomy 4p (4p15.1-->pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound.
    Chen CP; Hsu CY; Lee CC; Chen WL; Chen LF; Wang W
    Prenat Diagn; 2004 Nov; 24(11):934-6. PubMed ID: 15565589
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
    Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
    Boog G; Le Vaillant C; Collet M; Dupré PF; Parent P; Bongain A; Benoit B; Trastour C
    Fetal Diagn Ther; 2004; 19(5):421-30. PubMed ID: 15305099
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ultrasonographic findings of facial dysmorphism in Wolf-Hirschhorn syndrome.
    Sase M; Hasegawa K; Honda R; Sumie M; Nakata M; Sugino N; Furukawa S
    Am J Perinatol; 2005 Feb; 22(2):99-102. PubMed ID: 15731989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The 4P-syndrome. Case description and literature review.
    Moretti P; Ferrari M; Di Battista S; Di Battista C
    Minerva Pediatr; 2001 Feb; 53(1):23-8. PubMed ID: 11309539
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.
    Debost-Legrand A; Goumy C; Laurichesse-Delmas H; Déchelotte P; Beaufrère AM; Lémery D; Francannet C; Gallot D
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):806-11. PubMed ID: 24343879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).
    Chen CP; Lee MJ; Chern SR; Wu PS; Su JW; Chen YT; Lee MS; Wang W
    Gene; 2013 Oct; 529(2):351-6. PubMed ID: 23948085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Preaxial polydactyly in the 4p- syndrome.
    Schrander-Stumpel CT; Rijnvos WP; van der Blij-Philipsen M; Drogtrop A; Smeets D; Fryns JP
    Genet Couns; 1998; 9(1):63-5. PubMed ID: 9555593
    [No Abstract]   [Full Text] [Related]  

  • 13. [Wolf-Hirschhorn syndrome].
    Heljić S; Catibusić F; Dozić M; Mackić M
    Med Arh; 2004; 58(5):318-20. PubMed ID: 15628261
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
    Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
    Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of brain abnormalities in Wolf-Hirschhorn (4p-) syndrome.
    De Keersmaecker B; Albert M; Hillion Y; Ville Y
    Prenat Diagn; 2002 May; 22(5):366-70. PubMed ID: 12001188
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri-dimensional ultrasonography.
    Levaillant JM; Gérard-Blanluet M; Holder-Espinasse M; Valat-Rigot AS; Devisme L; Cavé H; Manouvrier-Hanu S
    Prenat Diagn; 2006 Apr; 26(4):340-4. PubMed ID: 16566035
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M; Martinovic J; Sanlaville D; Attié-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. Prenatal 3-dimensional sonographic depiction of the Wolf-Hirschhorn phenotype: the "Greek warrior helmet" and "tulip" signs.
    Sepulveda W
    J Ultrasound Med; 2007 Mar; 26(3):407-10. PubMed ID: 17324995
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Lee MS; Wang W
    Prenat Diagn; 2003 May; 23(5):375-9. PubMed ID: 12749033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.