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 *

115 related articles for article (PubMed ID: 26349185)

  • 1. MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.
    Gorukmez O; Gorukmez O; Sag OS; Yakut T; Gulten T
    Genet Couns; 2015; 26(2):163-9. PubMed ID: 26349185
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC
    Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW
    Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrasound diagnosis of central nervous system anomalies (bifid choroid plexus, ventriculomegaly, Dandy-Walker malformation) associated with multicystic dysplastic kidney disease in a trisomy 9 fetus: case report with literature review.
    Tonni G; Grisolia G
    J Clin Ultrasound; 2013 Sep; 41(7):441-7. PubMed ID: 23055272
    [TBL] [Abstract][Full Text] [Related]  

  • 5. "Understanding Adam" multiple reciprocal translocations: complex case presentation.
    Linder CE; Lu X; Kim YM; Li S; Pineda J
    J Perinat Neonatal Nurs; 2009; 23(2):150-6; quiz 157-8. PubMed ID: 19474586
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete trisomy 9 with unusual phenotypic associations: Dandy-Walker malformation, cleft lip and cleft palate, cardiovascular abnormalities.
    Tonni G; Lituania M; Chitayat D; Bonasoni MP; Keating S; Thompson M; Shannon P
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):592-7. PubMed ID: 25510707
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
    Chen CP; Liu FF; Jan SW; Yang YC; Lan CC
    Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomies of 8q and 15q due to maternal balanced translocations.
    Ozdemir M; Yuksel Z; Karaer K; Tekin N; Kucuk H; Erzurumluoglu E; Cilingir O
    Genet Couns; 2012; 23(3):375-82. PubMed ID: 23072185
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of partial trisomy 9p and the Dandy-Walker malformation.
    Chen CP; Chen CP; Shih JC
    Am J Med Genet A; 2005 Jan; 132A(1):111-2. PubMed ID: 15523627
    [No Abstract]   [Full Text] [Related]  

  • 13. Trisomy 18 with multiple rare malformations: report of one case.
    Su PH; Chen JY; Hsu CH; Chen SJ; Chan SW; Lin LL
    Acta Paediatr Taiwan; 2007; 48(5):272-5. PubMed ID: 18254577
    [TBL] [Abstract][Full Text] [Related]  

  • 14. First report of a small supernumerary der(8;14) marker chromosome.
    Guilherme RS; Dutra AR; Perez AB; Takeno SS; Oliveira MM; Kulikowski LD; Klein E; Hamid AB; Liehr T; Melaragno MI
    Cytogenet Genome Res; 2013; 139(4):284-8. PubMed ID: 23548553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
    Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
    Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS.
    Alp MY; Çebi AH; Seyhan S; Cansu A; Aydin H; Ikbal M
    Genet Couns; 2016; 27(1):43-9. PubMed ID: 27192891
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
    Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dandy-Walker malformation in an infant with tetrasomy 9p.
    Cazorla Calleja MR; Verdú A; Félix V
    Brain Dev; 2003 Apr; 25(3):220-3. PubMed ID: 12689705
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML; Ryan RM
    Am J Med Genet; 1995 Mar; 56(1):97-100. PubMed ID: 7747796
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
    Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.