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 *

231 related articles for article (PubMed ID: 15731989)

  • 21. Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia.
    van Dooren MF; Brooks AS; Hoogeboom AJ; van den Hoonaard TL; de Klein JE; Wouters CH; Tibboel D
    Am J Med Genet A; 2004 Jun; 127A(2):194-6. PubMed ID: 15108210
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo 4p-syndrome with oligohydramnios sequence.
    Su PH; Kuo PL; Chen SJ; Hung HM; Yi TH; Chen JY
    J Formos Med Assoc; 2003 Sep; 102(9):647-9. PubMed ID: 14625611
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Wolf-Hirschhorn syndrome in fetuses.
    Tachdjian G; Fondacci C; Tapia S; Huten Y; Blot P; Nessmann C
    Clin Genet; 1992 Dec; 42(6):281-7. PubMed ID: 1493641
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter.
    Chao A; Lee YS; Chao AS; Wang TH; Chang SD
    Birth Defects Res A Clin Mol Teratol; 2006 Oct; 76(10):739-43. PubMed ID: 17022067
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Pediatric diagnosis not made until adulthood: a case of Wolf-Hirschhorn syndrome.
    Coppola A; Chinthapalli K; Hammond P; Sander JW; Sisodiya SM
    Gene; 2013 Jan; 512(2):532-5. PubMed ID: 23064045
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP; Yang-Aisheng ; Kleczkowska A; Lemmens F; Vandecasseye W; van den Berghe H
    Ann Genet; 1989; 32(1):59-61. PubMed ID: 2751251
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies.
    Chen CP
    Genet Couns; 2007; 18(2):255-7. PubMed ID: 17710880
    [No Abstract]   [Full Text] [Related]  

  • 28. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
    Finzi S; Pinto CF; Wiggs JL
    Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
    Fryns JP; Smeets E; Devriendt K; Petit P
    Ann Genet; 1998; 41(2):73-6. PubMed ID: 9706336
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Wolf-Hirschhorn syndrome with posterior intraorbital coloboma cyst: an unusual case.
    Tutunculer F; Acunas B; Hicdonmez T; Deviren A; Pelitli V
    Brain Dev; 2004 Apr; 26(3):203-5. PubMed ID: 15030910
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Three-dimensional ultrasonographic visualization of fetal chromosome abnormalities: a preliminary experience report of 4 cases.
    Komwilaisak R; Ratanasiri T; Kleebkaow P
    J Med Assoc Thai; 2004 Oct; 87 Suppl 3():S38-44. PubMed ID: 21213493
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Wolf-Hirschhorn(4p-) syndrome.
    Mathai S; Ganguly BB
    Indian Pediatr; 2003 Jul; 40(7):681. PubMed ID: 12881629
    [No Abstract]   [Full Text] [Related]  

  • 37. Dissecting the Wolf-Hirschhorn syndrome phenotype: WHSC1 is a neurodevelopmental gene contributing to growth delay, intellectual disability, and to the facial dysmorphism.
    Zollino M; Doronzio PN
    J Hum Genet; 2018 Aug; 63(8):859-861. PubMed ID: 29884796
    [No Abstract]   [Full Text] [Related]  

  • 38. MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.
    Nieminen P; Kotilainen J; Aalto Y; Knuutila S; Pirinen S; Thesleff I
    J Dent Res; 2003 Dec; 82(12):1013-7. PubMed ID: 14630905
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Discrepancies in cytogenetic results between different tissues in two fetuses with Wolf- Hirschhorn syndrome.
    Schinzel A
    Cytogenet Cell Genet; 2000; 91(1-4):231-3. PubMed ID: 11173862
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.