BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 23918677)

  • 1. 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]  

  • 2. Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome due to disruption of BPTF in a 35-year-old man initially diagnosed with Silver-Russell syndrome.
    Midro AT; Tommerup N; Borys J; Panasiuk B; Kosztyła-Hojna B; Zalewska R; Konstantynowicz J; Łebkowska U; Cooper L; Scherer SE; Mehrjouy MM; Liu Q; Skowroński R; Stankiewicz P
    Clin Genet; 2019 Apr; 95(4):534-536. PubMed ID: 30633344
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

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

  • 6. Hepatomegaly and hyperammonemia in a girl with Silver-Russell syndrome caused by maternal uniparental isodisomy of chromosome 7.
    Li CF; Lin HY; Liu HC; Lee SH; Lo MY; Lin SP; Lo FS; Niu DM
    Am J Med Genet A; 2014 Aug; 164A(8):2114-7. PubMed ID: 24715348
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. A patient with Temple syndrome satisfying the clinical diagnostic criteria of Silver-Russell syndrome.
    Goto M; Kagami M; Nishimura G; Yamagata T
    Am J Med Genet A; 2016 Sep; 170(9):2483-5. PubMed ID: 27362607
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal sonographic features of Russell-Silver syndrome.
    Wax JR; Burroughs R; Wright MS
    J Ultrasound Med; 1996 Mar; 15(3):253-5. PubMed ID: 8919509
    [No Abstract]   [Full Text] [Related]  

  • 10. Silver-Russell Syndrome: A Review.
    Spiteri BS; Stafrace Y; Calleja-Agius J
    Neonatal Netw; 2017 Jul; 36(4):206-212. PubMed ID: 28764823
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Temple syndrome misdiagnosed as Silver-Russell syndrome.
    Luk HM
    Clin Dysmorphol; 2016 Apr; 25(2):82-3. PubMed ID: 26862943
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. [Russell Silver syndrome: report of three cases and review of the literature].
    Lamzouri A; Ratbi I; Sefiani A
    Pan Afr Med J; 2013; 14():91. PubMed ID: 23717707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Rare diseases with clinical relevance-the Silver-Russell syndrome].
    Neissner C; Schepp C; Rösch WH
    Urologe A; 2017 Jul; 56(7):876-881. PubMed ID: 28314972
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Unusual association of torticollis with Russell-Silver syndrome.
    Kaggare Puttaraju M; Manjunatha BS; Patil K; Kaiyoor LS
    BMJ Case Rep; 2023 May; 16(5):. PubMed ID: 37236674
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Russell-Silver Syndrome and Associated Feeding Challenges.
    Anderson S; Brill J; Kuchinski K
    J Pediatr Health Care; 2021; 35(6):630-638. PubMed ID: 34215464
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical utility gene card for: Silver-Russell syndrome.
    Eggermann T; Buiting K; Temple IK
    Eur J Hum Genet; 2011 Mar; 19(3):. PubMed ID: 21150879
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.