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 *

290 related articles for article (PubMed ID: 33920573)

  • 1. 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]  

  • 2. Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome.
    Pignata L; Sparago A; Palumbo O; Andreucci E; Lapi E; Tenconi R; Carella M; Riccio A; Cerrato F
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33923683
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.
    Inoue T; Yagasaki H; Nishioka J; Nakamura A; Matsubara K; Narumi S; Nakabayashi K; Yamazawa K; Fuke T; Oka A; Ogata T; Fukami M; Kagami M
    J Med Genet; 2019 Jun; 56(6):413-418. PubMed ID: 30242100
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
    Inoue T; Nakamura A; Iwahashi-Odano M; Tanase-Nakao K; Matsubara K; Nishioka J; Maruo Y; Hasegawa Y; Suzumura H; Sato S; Kobayashi Y; Murakami N; Nakabayashi K; Yamazawa K; Fuke T; Narumi S; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2020 Jun; 12(1):86. PubMed ID: 32546215
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients.
    Kawashima S; Nakamura A; Inoue T; Matsubara K; Horikawa R; Wakui K; Takano K; Fukushima Y; Tatematsu T; Mizuno S; Tsubaki J; Kure S; Matsubara Y; Ogata T; Fukami M; Kagami M
    J Clin Endocrinol Metab; 2018 Jun; 103(6):2083-2088. PubMed ID: 29878129
    [TBL] [Abstract][Full Text] [Related]  

  • 6. upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohorts.
    Hjortshøj TD; Sørensen AR; Yusibova M; Hansen BM; Dunø M; Balslev-Harder M; Grønskov K; van Hagen JM; Polstra AM; Eggermann T; Finken MJJ; Tümer Z
    Clin Genet; 2020 Jun; 97(6):902-907. PubMed ID: 32087029
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.
    Sachwitz J; Strobl-Wildemann G; Fekete G; Ambrozaitytė L; Kučinskas V; Soellner L; Begemann M; Eggermann T
    BMC Med Genet; 2016 Mar; 17():20. PubMed ID: 26969265
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system.
    Fuke T; Nakamura A; Inoue T; Kawashima S; Hara-Isono K; Matsubara K; Sano S; Yamazawa K; Fukami M; Ogata T; Kagami M
    J Hum Genet; 2022 Oct; 67(10):607-611. PubMed ID: 35606504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
    Kagami M; Mizuno S; Matsubara K; Nakabayashi K; Sano S; Fuke T; Fukami M; Ogata T
    Eur J Hum Genet; 2015 Aug; 23(8):1062-7. PubMed ID: 25351781
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13).
    Behnecke A; Hinderhofer K; Jauch A; Janssen JW; Moog U
    Clin Genet; 2012 Nov; 82(5):494-8. PubMed ID: 21954990
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Silver-Russell Syndrome - Part I: Clinical Characteristics and Genetic Background.
    Marczak-Hałupka A; Kalina MA; Tańska A; Chrzanowska KH
    Pediatr Endocrinol Diabetes Metab; 2015; 20(3):101-6. PubMed ID: 26615046
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.
    Vincent KM; Stavropoulos DJ; Beaulieu-Bergeron M; Yang C; Jiang M; Zuijdwijk C; Dyment DA; Graham GE
    Am J Med Genet A; 2022 Aug; 188(8):2421-2428. PubMed ID: 35593535
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The effects of 3-year growth hormone treatment and body composition in Polish patients with Silver-Russell syndrome.
    Świąder-Leśniak A; Jurkiewicz D; Kołodziejczyk H; Kozłowska A; Korpysz A; Szalecki M; Chrzanowska K
    Endokrynol Pol; 2023; 74(3):285-293. PubMed ID: 37335065
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome.
    Lin HY; Lee CL; Tu YR; Chang YH; Niu DM; Chang CY; Chiu PC; Chou YY; Hsiao HP; Tsai MC; Chao MC; Tsai LP; Yang CF; Su PH; Pan YW; Lee CH; Chu TH; Chuang CK; Lin SP
    Int J Med Sci; 2024; 21(1):8-18. PubMed ID: 38164354
    [No Abstract]   [Full Text] [Related]  

  • 15. Silver-Russell syndrome: genetic basis and molecular genetic testing.
    Eggermann T; Begemann M; Binder G; Spengler S
    Orphanet J Rare Dis; 2010 Jun; 5():19. PubMed ID: 20573229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndrome.
    Dias RP; Bogdarina I; Cazier JB; Buchanan C; Donaldson MC; Johnston LB; Hokken-Koelega AC; Clark AJ
    J Clin Endocrinol Metab; 2012 Nov; 97(11):E2188-93. PubMed ID: 22942387
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome.
    Fuke T; Mizuno S; Nagai T; Hasegawa T; Horikawa R; Miyoshi Y; Muroya K; Kondoh T; Numakura C; Sato S; Nakabayashi K; Tayama C; Hata K; Sano S; Matsubara K; Kagami M; Yamazawa K; Ogata T
    PLoS One; 2013; 8(3):e60105. PubMed ID: 23533668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome.
    Geoffron S; Abi Habib W; Chantot-Bastaraud S; Dubern B; Steunou V; Azzi S; Afenjar A; Busa T; Pinheiro Canton A; Chalouhi C; Dufourg MN; Esteva B; Fradin M; Geneviève D; Heide S; Isidor B; Linglart A; Morice Picard F; Naud-Saudreau C; Oliver Petit I; Philip N; Pienkowski C; Rio M; Rossignol S; Tauber M; Thevenon J; Vu-Hong TA; Harbison MD; Salem J; Brioude F; Netchine I; Giabicani E
    J Clin Endocrinol Metab; 2018 Jul; 103(7):2436-2446. PubMed ID: 29659920
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.