Results 121 to 130 of about 1,914,079 (159)

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

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

Silver City- Grant County Chamber of Commerce Collection; no.02056

Black and white image of two unidentified children standing and looking at a large formation of rocks, location at the City of Rocks. A late 30's or early 40's era automobile is parked in front of the rocks.
unknown
core  

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

Percutaneous endoscopic gastrostomy helped to normalise feeding problems and gastrointestinal symptoms in Silver-Russell syndrome. [PDF]

Acta Paediatr
Muz N, Petersson M, Saalman R, Dahlgren J.   +3 more
europepmc   +1 more source

Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylation. [PDF]

Front Pediatr
Darneau D, Giabicani E, Netchine I, Pham A.   +3 more
europepmc   +1 more source

Prenatal diagnosis of Silver-Russell syndrome with 8q12 deletion including the PLAG1 gene: a case report and review. [PDF]

Front Genet
Wu K, Zhu Y, Zhu Q.
europepmc   +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

Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.

J Clin Endocrinol Metab
Vimercati A, Tannorella P, Guzzetti S, Calzari L, Gentilini D, Manfredini E, Gori G, Gaudino R, Antona V, Piccione M, Daolio C, Auricchio R, Sirchia F, Minelli A, Rossi E, Bellini M, Biasucci G, Raucci AR, Pozzobon G, Patti G, Napoli F, Larizza L, Maghnie M, Russo S.   +23 more
europepmc   +1 more source