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 *

165 related articles for article (PubMed ID: 35169783)

  • 21. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
    Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
    Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
    [TBL] [Abstract][Full Text] [Related]  

  • 22. BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1.
    Brunet A; Armengol L; Heine D; Rosell J; García-Aragonés M; Gabau E; Estivill X; Guitart M
    BMC Med Genet; 2009 Dec; 10():144. PubMed ID: 20030804
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.
    Dempsey MA; Schwartz S; Waggoner DJ
    Am J Med Genet A; 2007 May; 143A(10):1082-6. PubMed ID: 17431914
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
    Busè M; Cuttaia HC; Palazzo D; Mazara MV; Lauricella SA; Malacarne M; Pierluigi M; Cavani S; Piccione M
    Ital J Pediatr; 2017 Jul; 43(1):61. PubMed ID: 28724436
    [TBL] [Abstract][Full Text] [Related]  

  • 25. An unusual combination of an atypical maternally inherited novel 0.3 Mb deletion in Williams-Beuren region and a de novo 22q11.21 microduplication in an infant with supravalvular aortic stenosis.
    Evangelidou P; Kousoulidou L; Salameh N; Alexandrou A; Papaevripidou I; Alexandrou IM; Ketoni A; Ioannidou C; Christophidou-Anastasiadou V; Tanteles GA; Sismani C
    Eur J Med Genet; 2020 Dec; 63(12):104084. PubMed ID: 33045407
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment.
    Pebrel-Richard C; Kemeny S; Gouas L; Eymard-Pierre E; Blanc N; Francannet C; Tchirkov A; Goumy C; Vago P
    Eur J Med Genet; 2012 Nov; 55(11):650-5. PubMed ID: 22796526
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
    Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
    BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Microduplication 22q11.2: a new chromosomal syndrome.
    Portnoï MF
    Eur J Med Genet; 2009; 52(2-3):88-93. PubMed ID: 19254783
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.
    Cuturilo G; Menten B; Krstic A; Drakulic D; Jovanovic I; Parezanovic V; Stevanovic M
    Eur J Pediatr; 2011 Nov; 170(11):1465-70. PubMed ID: 21833498
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment.
    Lundin J; Söderhäll C; Lundén L; Hammarsjö A; White I; Schoumans J; Läckgren G; Kockum CC; Nordenskjöld A
    Eur J Med Genet; 2010; 53(2):61-5. PubMed ID: 20045748
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genotypic and phenotypic variability of 22q11.2 microdeletions - an institutional experience.
    Manno GC; Segal GS; Yu A; Xu F; Ray JW; Cooney E; Britt AD; Jain SK; Goldblum RM; Robinson SS; Dong J
    AIMS Mol Sci; 2021; 8(4):257-274. PubMed ID: 34938854
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome.
    Prescott K; Woodfine K; Stubbs P; Super M; Kerr B; Palmer R; Carter NP; Scambler P
    Hum Genet; 2005 Jan; 116(1-2):83-90. PubMed ID: 15549396
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
    Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
    Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance.
    Woodward KJ; Stampalia J; Vanyai H; Rijhumal H; Potts K; Taylor F; Peverall J; Grumball T; Sivamoorthy S; Alinejad-Rokny H; Wray J; Whitehouse A; Nagarajan L; Scurlock J; Afchani S; Edwards M; Murch A; Beilby J; Baynam G; Kiraly-Borri C; McKenzie F; Heng JIT
    Mol Genet Genomic Med; 2019 Feb; 7(2):e00507. PubMed ID: 30614210
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
    Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
    Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Atypical copy number abnormalities in 22q11.2 region: report of three cases.
    Molck MC; Vieira TP; Sgardioli IC; Simioni M; Dos Santos AP; Souza J; Monteiro FP; Gil-da-Silva-Lopes VL
    Eur J Med Genet; 2013 Sep; 56(9):515-20. PubMed ID: 23886712
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
    Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T
    Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cytogenomic Evaluation of Children with Congenital Anomalies: Critical Implications for Diagnostic Testing and Genetic Counseling.
    Szczałuba K; Jakubiuk-Tomaszuk A; Kędzior M; Bernaciak J; Zdrodowska J; Kurzątkowski W; Radkowski M; Demkow U
    Adv Exp Med Biol; 2016; 912():11-9. PubMed ID: 26987321
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Comparative genomic hybridization analysis of genomic alterations in benign, atypical and anaplastic meningiomas.
    Arslantas A; Artan S; Oner U; Durmaz R; Müslümanoğlu H; Atasoy MA; Başaran N; Tel E
    Acta Neurol Belg; 2002 Jun; 102(2):53-62. PubMed ID: 12161900
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.