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 *

136 related articles for article (PubMed ID: 23065819)

  • 1. Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.
    Wadt K; Jensen LN; Bjerglund L; Lundstrøm M; Kirchhoff M; Kjaergaard S
    Prenat Diagn; 2012 Dec; 32(12):1212-7. PubMed ID: 23065819
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1.
    Engwerda A; Kerstjens-Frederikse WS; Corsten-Janssen N; Dijkhuizen T; van Ravenswaaij-Arts CMA
    Orphanet J Rare Dis; 2023 Mar; 18(1):59. PubMed ID: 36935482
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 6q deletions: a report of two additional cases and a review of the literature.
    McLeod DR; Fowlow SB; Robertson A; Samcoe D; Burgess I; Hoo JJ
    Am J Med Genet; 1990 Jan; 35(1):79-84. PubMed ID: 2405671
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.
    Narahara K; Tsuji K; Yokoyama Y; Namba H; Murakami M; Matsubara T; Kasai R; Fukushima Y; Seki T; Wakui K
    Am J Med Genet; 1991 Sep; 40(3):348-53. PubMed ID: 1951444
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expanding the clinical and neuroradiological phenotype of 6q27 microdeletion: olfactory bulb aplasia and anosmia.
    Gerber JC; Neuhann TM; Tyshchenko N; Smitka M; Hackmann K
    Am J Med Genet A; 2011 Aug; 155A(8):1981-6. PubMed ID: 21744487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unusual Form of Obstructive Hydrocephalus in Association with 6q Terminal Deletion Syndrome: A Case Report and Literature Review.
    Iwamoto H; Muroi A; Sekine T; Tsurubuchi T; Ishikawa E; Matsumura A
    Pediatr Neurosurg; 2019; 54(6):419-423. PubMed ID: 31597145
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome.
    Backx L; Fryns JP; Marcelis C; Devriendt K; Vermeesch J; Van Esch H
    Am J Med Genet A; 2010 Feb; 152A(2):319-26. PubMed ID: 20082458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A de novo 3.54 Mb deletion of 17q22-q23.1 associated with hydrocephalus: a case report and review of literature.
    Khattab M; Xu F; Li P; Bhandari V
    Am J Med Genet A; 2011 Dec; 155A(12):3082-6. PubMed ID: 22052796
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New insights into the phenotypes of 6q deletions.
    Hopkin RJ; Schorry E; Bofinger M; Milatovich A; Stern HJ; Jayne C; Saal HM
    Am J Med Genet; 1997 Jun; 70(4):377-86. PubMed ID: 9182778
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Report of two cases of distal deletion of the long arm of chromosome 6.
    Stevens CA; Fineman RM; Breg WR; Silken AB
    Am J Med Genet; 1988 Apr; 29(4):807-14. PubMed ID: 3400725
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.
    Sosoi S; Streata I; Tudorache S; Burada F; Siminel M; Cernea N; Ioana M; Iliescu DG; Mixich F
    J Hum Genet; 2015 Apr; 60(4):183-5. PubMed ID: 25652353
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A de novo proximal 6q deletion confirmed by array comparative genomic hybridization.
    Woo KS; Kim JE; Kim KE; Kim MJ; Yoo JH; Ahn HS; Shaffer LG; Han JY
    Korean J Lab Med; 2010 Feb; 30(1):84-8. PubMed ID: 20197728
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.
    Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Wang W
    Gene; 2013 Mar; 516(1):138-42. PubMed ID: 23266815
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.
    Sung PL; Chang CM; Chen CY; Wang PH; Chao KC; Wen KC; Cheng YY; Li YC; Lin CC
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):260-5. PubMed ID: 22795105
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genomic detection of a familial 382 Kb 6q27 deletion in a fetus with isolated severe ventriculomegaly and her affected mother.
    Thakur M; Bronshtein E; Hankerd M; Adekola H; Puder K; Gonik B; Ebrahim S
    Am J Med Genet A; 2018 Sep; 176(9):1985-1990. PubMed ID: 30194807
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The natural history of prenatally diagnosed cerebral ventriculomegaly.
    Drugan A; Krause B; Canady A; Zador IE; Sacks AJ; Evans MI
    JAMA; 1989 Mar 24-31; 261(12):1785-8. PubMed ID: 2645455
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements.
    Souter VL; Glass IA; Chapman DB; Raff ML; Parisi MA; Opheim KE; Disteche CM
    Ultrasound Obstet Gynecol; 2003 Jun; 21(6):609-15. PubMed ID: 12808681
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.