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 *

157 related articles for article (PubMed ID: 12011164)

  • 1. Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints.
    Kocks A; Endele S; Heller R; Schröder B; Schäfer HJ; Städtler C; Makrigeorgi-Butera M; Winterpacht A
    J Med Genet; 2002 May; 39(5):E23. PubMed ID: 12011164
    [No Abstract]   [Full Text] [Related]  

  • 2. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
    Laleye A; Alao MJ; Adjagba M; Hans C; Delneste D; Gnamey DK; Ayivi B; Darboux RB
    Genet Couns; 2006; 17(1):35-40. PubMed ID: 16719275
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.
    Guilherme RS; Bragagnolo S; Pellegrino R; Christofolini DM; Takeno SS; Carvolheira GM; Kulikowski LD; Melaragno MI
    Cytogenet Genome Res; 2011; 134(4):325-30. PubMed ID: 21849783
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report.
    Sandal G; Ormeci AR; Oztas S
    Genet Couns; 2013; 24(2):217-22. PubMed ID: 24032293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome.
    Seller MJ; Pal K; Docherty Z; Nash TG
    Clin Dysmorphol; 1994 Jan; 3(1):35-9. PubMed ID: 8205324
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 4q21 microdeletion in a patient with epilepsy and brain malformations.
    Yano S; McNamara M; Halbach S; Waggoner D
    Am J Med Genet A; 2015 Jun; 167(6):1409-13. PubMed ID: 25847229
    [No Abstract]   [Full Text] [Related]  

  • 8. [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion].
    Kim JH; Oh PS; Na HY; Kim SH; Cho HC
    Korean J Lab Med; 2009 Feb; 29(1):77-81. PubMed ID: 19262083
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay.
    Blackett PR; Li S; Mulvihill JJ
    Am J Med Genet A; 2005 Aug; 137(2):213-6. PubMed ID: 16082703
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome.
    Tsang E; Rupps R; McGillivray B; Eydoux P; Marra M; Arbour L; Langlois S; Friedman JM; Zahir FR
    Am J Med Genet A; 2012 Oct; 158A(10):2606-9. PubMed ID: 22903878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation.
    Kellermayer R; Gyarmati J; Czakó M; Tészás A; Masszi G; Ertl T; Kosztolányi G
    Am J Med Genet A; 2005 Dec; 139(3):234-5. PubMed ID: 16278901
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients.
    Repetto GM; Guzmán ML; Puga A; Calderón JF; Astete CP; Aracena M; Arriaza M; Aravena T; Sanz P
    Clin Genet; 2009 Nov; 76(5):465-70. PubMed ID: 19737282
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction.
    Lin YH; Chen CP; Chen TC; Hsu CS; Chou SY; Chien SC
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):528-30. PubMed ID: 22212331
    [No Abstract]   [Full Text] [Related]  

  • 14. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
    Nowaczyk MJ; Ramsay JA; Mohide P; Tomkins DJ
    Am J Med Genet; 1998 May; 77(4):306-9. PubMed ID: 9600741
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Bilateral absence of the ulna in 4q terminal deletion syndrome: evidence for a critical region.
    Meaux T; Zeringue A; Mumphrey C; Barkemeyer B; Marble M
    Clin Dysmorphol; 2015 Jul; 24(3):122-4. PubMed ID: 25719425
    [No Abstract]   [Full Text] [Related]  

  • 17. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes.
    Aldred MA; Sanford RO; Thomas NS; Barrow MA; Wilson LC; Brueton LA; Bonaglia MC; Hennekam RC; Eng C; Dennis NR; Trembath RC
    J Med Genet; 2004 Jun; 41(6):433-9. PubMed ID: 15173228
    [No Abstract]   [Full Text] [Related]  

  • 19. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss.
    Sakazume S; Kido Y; Murakami N; Matsubara T; Numabe H
    Pediatr Int; 2015 Oct; 57(5):880-3. PubMed ID: 26114601
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.