Results 161 to 170 of about 58,780 (225)

Clinical Application of Sequential Epigenetic Analysis for Diagnosis of Silver-Russell Syndrome. [PDF]

Ann Lab Med, 2021
Kim SY, Shin CH, Lee YA, Shin CH, Yang SW, Cho TJ, Ko JM.   +6 more
europepmc   +1 more source

World small animal veterinary association renal pathology initiative: classification of glomerular diseases in dogs [PDF]

, 2015
Aresu, L, Brovida, C, Brown, C A, Cianciolo, R E, Cowgill, L D, Heiene, R, James, C, Jansen, J H, Kass, PH, Lees, G E, Mohr, F C, Polzin, D J, Spangler, W L, Syme, H M, Vaden, S L, van de Lugt, JJ, van Dongen, A M   +16 more
core   +2 more sources

Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome. [PDF]

Mol Syndromol, 2021
Lengyel A, Pinti É, Eggermann T, Fekete G, Haltrich I.   +4 more
europepmc   +1 more source

Prenatal Silver-Russell Syndrome in a Chinese Family Identified by Non-Invasive Prenatal Testing. [PDF]

Mol Syndromol, 2022
Zhang YL, Jing XY, Wan JH, Pan M, Li DZ.
europepmc   +1 more source

Prenatal diagnosis of a silver-russell syndrome caused by 11p15 duplication and pedigree analysis. [PDF]

Front Genet
Hong S, Wei H, Zhuang X, Huang W, Zhang Y.   +4 more
europepmc   +1 more source

Washington University Medical Alumni Quarterly, January 1950 [PDF]

, 1950

core   +1 more source

Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7. [PDF]

Front Endocrinol (Lausanne)
Shoji T, Yamauchi I, Kawasaki H, Iwanaga K, Hakata T, Tanaka D, Fujikura J, Masui T, Suzuki H, Yamada M, Kosaki K, Kasai Y, Hatano E, Inaba A, Wada T, Kosugi S, Ueda Y, Fujii T, Taura D, Inagaki N.   +19 more
europepmc   +1 more source

Correction to: "Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene". [PDF]

J Clin Endocrinol Metab
europepmc   +1 more source

Guidance for schools : recording children with special educational needs : SEN categories [PDF]

, 2006

core  

Erratum: Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum. [PDF]

Front Genet
Frontiers Production Office.
europepmc   +1 more source