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Year | Number of Results |
---|---|
2015 | 1 |
2017 | 3 |
2018 | 2 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
PubMed (cited) for id: 616489
7 results
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Page 1
IGF2 Mutations.
J Clin Endocrinol Metab. 2020 Jan 1;105(1):dgz034. doi: 10.1210/clinem/dgz034.
J Clin Endocrinol Metab. 2020.
PMID: 31544945
Review.
A new p.(Ile66Serfs*93) IGF2 variant is associated with pre- and postnatal growth retardation.
Rockstroh D, Pfäffle H, Le Duc D, Rößler F, Schlensog-Schuster F, Heiker JT, Kratzsch J, Kiess W, Lemke JR, Abou Jamra R, Pfäffle R.
Rockstroh D, et al.
Eur J Endocrinol. 2019 Jan 1;180(1):K1-K13. doi: 10.1530/EJE-18-0601.
Eur J Endocrinol. 2019.
PMID: 30400067
Item in Clipboard
Silver Russel syndrome in an aboriginal patient from Australia.
Poulton C, Azmanov D, Atkinson V, Beilby J, Ewans L, Gration D, Dreyer L, Shetty V, Peake C, McCormack E, Palmer R, Lewis B, Dawkins H, Broley S, Baynam G.
Poulton C, et al.
Am J Med Genet A. 2018 Dec;176(12):2561-2563. doi: 10.1002/ajmg.a.40502. Epub 2018 Aug 27.
Am J Med Genet A. 2018.
PMID: 30152198
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De Novo Mutation of Paternal IGF2 Gene Causing Silver-Russell Syndrome in a Sporadic Patient.
Liu D, Wang Y, Yang XA, Liu D.
Liu D, et al.
Front Genet. 2017 Aug 8;8:105. doi: 10.3389/fgene.2017.00105. eCollection 2017.
Front Genet. 2017.
PMID: 28848601
Free PMC article.
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Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.
Abi Habib W, Brioude F, Edouard T, Bennett JT, Lienhardt-Roussie A, Tixier F, Salem J, Yuen T, Azzi S, Le Bouc Y, Harbison MD, Netchine I.
Abi Habib W, et al.
Genet Med. 2018 Feb;20(2):250-258. doi: 10.1038/gim.2017.105. Epub 2017 Aug 10.
Genet Med. 2018.
PMID: 28796236
Free PMC article.
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De novo IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactyly.
Yamoto K, Saitsu H, Nakagawa N, Nakajima H, Hasegawa T, Fujisawa Y, Kagami M, Fukami M, Ogata T.
Yamoto K, et al.
Hum Mutat. 2017 Aug;38(8):953-958. doi: 10.1002/humu.23253. Epub 2017 May 29.
Hum Mutat. 2017.
PMID: 28489339
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Paternally Inherited IGF2 Mutation and Growth Restriction.
Begemann M, Zirn B, Santen G, Wirthgen E, Soellner L, Büttel HM, Schweizer R, van Workum W, Binder G, Eggermann T.
Begemann M, et al.
N Engl J Med. 2015 Jul 23;373(4):349-56. doi: 10.1056/NEJMoa1415227. Epub 2015 Jul 8.
N Engl J Med. 2015.
PMID: 26154720
Free article.
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