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 *

116 related articles for article (PubMed ID: 30556288)

  • 1. Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype.
    Kanani F; Parker MJ; Burren CP; Rankin J; Balasubramanian M
    Am J Med Genet A; 2019 Jan; 179(1):139-140. PubMed ID: 30556288
    [No Abstract]   [Full Text] [Related]  

  • 2. Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome.
    Cytrynbaum C; Chong K; Hannig V; Choufani S; Shuman C; Steele L; Morgan T; Scherer SW; Stavropoulos DJ; Basran RK; Weksberg R
    Am J Med Genet A; 2016 Oct; 170(10):2731-9. PubMed ID: 27374371
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Silver-Russell syndrome in Hong Kong.
    Luk HM; Yeung KS; Wong WL; Chung BH; Tong TM; Lo IF
    Hong Kong Med J; 2016 Dec; 22(6):526-33. PubMed ID: 27468965
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Absent digit in Russell-Silver syndrome: expanding the clinical spectrum of a well known syndrome.
    Strong A; McDougall C; Zackai E
    Clin Dysmorphol; 2020 Apr; 29(2):118-120. PubMed ID: 31895057
    [No Abstract]   [Full Text] [Related]  

  • 6. The next generation of Silver-Russell syndrome.
    Welch TR
    J Pediatr; 2017 Aug; 187():3-4. PubMed ID: 28750761
    [No Abstract]   [Full Text] [Related]  

  • 7. Epigenetic signatures of Silver-Russell syndrome.
    Abu-Amero S; Wakeling EL; Preece M; Whittaker J; Stanier P; Moore GE
    J Med Genet; 2010 Mar; 47(3):150-4. PubMed ID: 20305090
    [No Abstract]   [Full Text] [Related]  

  • 8. New developments in Silver-Russell syndrome and implications for clinical practice.
    Ishida M
    Epigenomics; 2016 Apr; 8(4):563-80. PubMed ID: 27066913
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Type 1 collagenopathy presenting with a Russell-Silver phenotype.
    Parker MJ; Deshpande C; Rankin J; Wilson LC; Balasubramanian M; Hall CM; Wagner BE; Pollitt R; Dalton A; Bishop NJ
    Am J Med Genet A; 2011 Jun; 155A(6):1414-8. PubMed ID: 21567925
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic Analysis and Clinical Presentation in Silver Russell Syndrome.
    Lohiya N; Lote-Oke R; Agarwal M; Phadke N; Khadilkar V; Khadilkar A
    Indian J Pediatr; 2018 Dec; 85(12):1141-1142. PubMed ID: 30039337
    [No Abstract]   [Full Text] [Related]  

  • 11. Russel-Silver syndrome: A historical note and comment on an older adult.
    Searle C; Johnson D
    Am J Med Genet A; 2016 Feb; 170A(2):466-470. PubMed ID: 26525433
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mosaic upd(7)mat in a patient with Silver-Russell syndrome.
    Fuke-Sato T; Yamazawa K; Nakabayashi K; Matsubara K; Matsuoka K; Hasegawa T; Dobashi K; Ogata T
    Am J Med Genet A; 2012 Feb; 158A(2):465-8. PubMed ID: 22246578
    [No Abstract]   [Full Text] [Related]  

  • 13. Isolated hypermethylation of GRB10 (7p12.2) in a Silver-Russell syndrome patient carrying a 20p13 microdeletion.
    Eggermann T; Schneider-Rätzke B; Begemann M; Spengler S
    Clin Genet; 2014 Apr; 85(4):399-400. PubMed ID: 23745689
    [No Abstract]   [Full Text] [Related]  

  • 14. Epigenetic and genetic diagnosis of Silver-Russell syndrome.
    Eggermann T; Spengler S; Gogiel M; Begemann M; Elbracht M
    Expert Rev Mol Diagn; 2012 Jun; 12(5):459-71. PubMed ID: 22702363
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Collagenopathy with a phenotype resembling Silver-Russell syndrome phenotype.
    Cianci P; Paterlini G; Tagliabue P; Verderio M; Vergani P; Bianchi ML; Giussani C; Kullmann G; Mazzoleni F; Bozzetti A; Selicorni A
    Am J Med Genet A; 2013 Oct; 161A(10):2681-4. PubMed ID: 23918677
    [No Abstract]   [Full Text] [Related]  

  • 16. Germline correction of an epimutation related to Silver-Russell syndrome.
    Bruno C; Carmignac V; Netchine I; Choux C; Duffourd Y; Faivre L; Thauvin-Robinet C; Le Bouc Y; Sagot P; Bourc'his D; Fauque P
    Hum Mol Genet; 2015 Jun; 24(12):3314-21. PubMed ID: 25736213
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7.
    Stark Z; Ryan MM; Bruno DL; Burgess T; Savarirayan R
    Am J Med Genet A; 2010 Sep; 152A(9):2342-5. PubMed ID: 20684011
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Left Second Metacarpal Pseudoepiphysis in Silver-Russell Syndrome.
    Ranasinghe JC; Thambavita W
    Indian J Pediatr; 2021 Oct; 88(10):1040-1041. PubMed ID: 34018134
    [No Abstract]   [Full Text] [Related]  

  • 20. Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome.
    Wu D; Gong C; Su C
    Sci China Life Sci; 2017 Jul; 60(7):692-699. PubMed ID: 28624953
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.