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 *

190 related articles for article (PubMed ID: 26921528)

  • 1. The use of two different MLPA kits in 22q11.2 deletion syndrome.
    Evers LJ; Engelen JJ; Houben LM; Curfs LM; van Amelsvoort TA
    Eur J Med Genet; 2016 Apr; 59(4):183-8. PubMed ID: 26921528
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
    Demily C; Rossi M; Schneider M; Edery P; Leleu A; d'Amato T; Franck N; Eliez S
    Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [An attempt to identify 22q11.2 microdeletions in samples of the Hungarian schizophrenia DNA bank by multiplex ligation-based probe amplification (MLPA): literature review, methodology and results].
    Klein I; Szocs K; Vincze K; Benkovits J; Somogyi S; Herman L; Rethelyi JM
    Neuropsychopharmacol Hung; 2016 Dec; 18(4):209-218. PubMed ID: 28259864
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification.
    Stachon AC; Baskin B; Smith AC; Shugar A; Cytrynbaum C; Fishman L; Mendoza-Londono R; Klatt R; Teebi A; Ray PN; Weksberg R
    Am J Med Genet A; 2007 Dec; 143A(24):2924-30. PubMed ID: 18000985
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability.
    Evers LJ; van Amelsvoort TA; Candel MJ; Boer H; Engelen JJ; Curfs LM
    J Intellect Disabil Res; 2014 Oct; 58(10):915-25. PubMed ID: 24528781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome.
    Jensen M; Kooy RF; Simon TJ; Reyniers E; Girirajan S; Tassone F
    Eur J Med Genet; 2018 Apr; 61(4):209-212. PubMed ID: 29191496
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detailed analysis of 22q11.2 with a high density MLPA probe set.
    Jalali GR; Vorstman JA; Errami A; Vijzelaar R; Biegel J; Shaikh T; Emanuel BS
    Hum Mutat; 2008 Mar; 29(3):433-40. PubMed ID: 18033723
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population.
    Loghmani Khouzani H; Kariminejad A; Zamani G; Ghalandary M; Bozorgmehr B; Amirsalari S; Mojahedi F; Tonekaboni SH; Kariminejad R; Najmabadi H
    Arch Iran Med; 2014 Jul; 17(7):471-4. PubMed ID: 24979557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.
    Vergaelen E; Swillen A; Van Esch H; Claes S; Van Goethem G; Devriendt K
    Eur J Med Genet; 2015 Apr; 58(4):244-8. PubMed ID: 25655469
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
    Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
    BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.
    Fernández L; Lapunzina P; Arjona D; López Pajares I; García-Guereta L; Elorza D; Burgueros M; De Torres ML; Mori MA; Palomares M; García-Alix A; Delicado A
    Clin Genet; 2005 Oct; 68(4):373-8. PubMed ID: 16143025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rearrangement in 22q11 implicated in Iranian patients with mental retardation.
    Mona M; Mehrdad N; Mehrdad B; Elham N; Khazamipour N
    Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1604-9. PubMed ID: 22939590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting.
    Zhang X; Wang B; Zhang L; You G; Palais RA; Zhou L; Fu Q
    BMC Genomics; 2018 Jun; 19(1):485. PubMed ID: 29925309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genotype and phenotype studies on fetuses of 22q11.2 deletion syndrome].
    Zhu H; Zhang Y; Ji C; Li S; Niu Y; Zhang H; Chen L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):721-724. PubMed ID: 32619250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Relationship between reaction time, fine motor control, and visual-spatial perception on vigilance and visual-motor tasks in 22q11.2 Deletion Syndrome.
    Howley SA; Prasad SE; Pender NP; Murphy KC
    Res Dev Disabil; 2012; 33(5):1495-502. PubMed ID: 22522207
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
    Gavril EC; Popescu R; Nucă I; Ciobanu CG; Butnariu LI; Rusu C; Pânzaru MC
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36360320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Rare Etiology of Hypocalcemic Seizures in Adulthood: Clues to Diagnosis from Facial Dysmorphism.
    Batra N; Kant R; Mandal K; Joshi K
    Neurol India; 2021; 69(1):161-163. PubMed ID: 33642291
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic and clinical characteristics of 22q11.2 deletion syndrome].
    Kozlova IuO; Zabnenkova VV; Shilova NV; Min'zhenkova ME; Antonenko VG; Kotlukova NP; Simonova LV; Kazanceva IA; Levchenko EG; Bombardirova TD; Zolotukhina TV; Poliakov AV
    Genetika; 2014 May; 50(5):602-10. PubMed ID: 25715476
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
    Mademont-Soler I; Morales C; Soler A; Clusellas N; Margarit E; Martínez-Barrios E; Martínez JM; Sánchez A
    Gene; 2012 May; 500(1):151-4. PubMed ID: 22446045
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.