Results 161 to 170 of about 58,220 (206)

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 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

Hemofiltration in human sepsis [PDF]

, 1994
Deppisch, R., Faist, E., Hartl, W. H., Hoffmann, J. N., Inthorn, D., Jochum, Marianne   +5 more
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

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

Washington University Medical Alumni Quarterly, July 1951 [PDF]

, 1951

core   +1 more source

P236: Familial Russell-Silver syndrome: Hypomethylation of imprinting center 1 in two siblings

Genetics in Medicine Open
Kendra Engleman, Ana S.A. Cohen, Joseph Alaimo, Bonnie Sullivan   +3 more
doaj   +1 more source

Washington University Medical Alumni Quarterly, January 1950 [PDF]

, 1950

core   +1 more source