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 *

140 related articles for article (PubMed ID: 34480472)

  • 1. Silver Russell syndrome in a preterm girl with 8q12.1 deletion encompassing PLAG1.
    Fernández-Fructuoso JR; De la Torre-Sandoval C; Harbison MD; Chantot-Bastaraud S; Temple K; Lloreda-Garcia JM; Olmo-Sanchez M; Netchine I
    Clin Dysmorphol; 2021 Oct; 30(4):194-196. PubMed ID: 34480472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.
    Brereton RE; Nickerson SL; Woodward KJ; Edwards T; Sivamoorthy S; Ramos Vasques Walters F; Chabros V; Marchin V; Grumball T; Kennedy D; Uzaraga J; Peverall J; Arscott G; Beilby J; Choong CS; Townshend S; Azmanov DN
    Am J Med Genet A; 2021 Oct; 185(10):3136-3145. PubMed ID: 34223693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes.
    Baba N; Lengyel A; Pinti E; Yapici E; Schreyer I; Liehr T; Fekete G; Eggermann T
    Mol Cytogenet; 2022 May; 15(1):19. PubMed ID: 35562807
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel Variant in
    Vado Y; Pereda A; Llano-Rivas I; Gorria-Redondo N; Díez I; Perez de Nanclares G
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33291420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of Silver-Russell syndrome with 8q12 deletion including the
    Wu K; Zhu Y; Zhu Q
    Front Genet; 2024; 15():1387649. PubMed ID: 38826801
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case report: Long term response to growth hormone in a child with Silver-Russell syndrome-like phenotype due to a novel paternally inherited IGF2 variant.
    Ventresca S; Lepri FR; Criscuolo S; Bottaro G; Novelli A; Loche S; Cappa M
    Front Endocrinol (Lausanne); 2024; 15():1364234. PubMed ID: 38596219
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternally inherited autosomal dominant PLAG-1 related Silver Russell syndrome in a fetus with intra-uterine growth restriction.
    Tse WT; Bass C; Gurney L; Kinning E
    Prenat Diagn; 2023 Jun; 43(6):724-726. PubMed ID: 37165482
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature.
    Mercadante F; Busè M; Salzano E; Fragapane T; Palazzo D; Malacarne M; Piccione M
    Ital J Pediatr; 2020 Jul; 46(1):108. PubMed ID: 32723361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS features.
    Sachwitz J; Meyer R; Fekete G; Spranger S; Matulevičienė A; Kučinskas V; Bach A; Luczay A; Brüchle NO; Eggermann K; Zerres K; Elbracht M; Eggermann T
    Clin Genet; 2017 Jan; 91(1):73-78. PubMed ID: 27172843
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases.
    Tannorella P; Minervino D; Guzzetti S; Vimercati A; Calzari L; Patti G; Maghnie M; Allegri AEM; Milani D; Scuvera G; Mariani M; Modena P; Selicorni A; Larizza L; Russo S
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33920573
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Silver Russel syndrome in an aboriginal patient from Australia.
    Poulton C; Azmanov D; Atkinson V; Beilby J; Ewans L; Gration D; Dreyer L; Shetty V; Peake C; McCormack E; Palmer R; Lewis B; Dawkins H; Broley S; Baynam G
    Am J Med Genet A; 2018 Dec; 176(12):2561-2563. PubMed ID: 30152198
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization.
    Cocchi G; Marsico C; Cosentino A; Spadoni C; Rocca A; De Crescenzo A; Riccio A
    Am J Med Genet A; 2013 Oct; 161A(10):2652-5. PubMed ID: 24038823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.
    Abi Habib W; Brioude F; Edouard T; Bennett JT; Lienhardt-Roussie A; Tixier F; Salem J; Yuen T; Azzi S; Le Bouc Y; Harbison MD; Netchine I
    Genet Med; 2018 Feb; 20(2):250-258. PubMed ID: 28796236
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microdeletions of the 7q32.2 imprinted region are associated with Silver-Russell syndrome features.
    Carrera IA; de Zaldívar MS; Martín R; Begemann M; Soellner L; Eggermann T
    Am J Med Genet A; 2016 Mar; 170(3):743-9. PubMed ID: 26663145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A boy with Silver-Russell syndrome and Sotos syndrome.
    Schwaibold EMC; Beygo J; Obeid K; Jauch A; Hinderhofer K; Moog U
    Am J Med Genet A; 2021 Feb; 185(2):549-554. PubMed ID: 33191647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical characterization of PLAG1- related Silver-Russell syndrome:A clinical report.
    Dong P; Zhang N; Zhang Y; Liu CX; Li CL
    Eur J Med Genet; 2023 Oct; 66(10):104837. PubMed ID: 37673301
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver-Russell syndrome.
    Dateki S; Kagami M; Matsubara K; Izumi K; Watanabe S; Nakatomi A; Kondoh T; Fukami M; Moriuchi H
    J Hum Genet; 2017 Oct; 62(10):919-922. PubMed ID: 28592837
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Silver-Russell syndrome.
    Wakeling EL
    Arch Dis Child; 2011 Dec; 96(12):1156-61. PubMed ID: 21349887
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
    Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.
    Inoue T; Nakamura A; Fuke T; Yamazawa K; Sano S; Matsubara K; Mizuno S; Matsukura Y; Harashima C; Hasegawa T; Nakajima H; Tsumura K; Kizaki Z; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2017; 9():52. PubMed ID: 28515796
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.