Wilms tumor in patients with osteopathia striata with cranial sclerosis-Reference-Cited by-同舟云学术

Wilms tumor in patients with osteopathia striata with cranial sclerosis

Published:2020-09-02 Issue:3 Volume:29 Page:396-401
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Bach Alicia^ORCID,Mi Jingyi,Hunter Matthew,Halliday Benjamin J.,García-Miñaúr Sixto,Sperotto Francesca^ORCID,Trevisson Eva^ORCID,Markie David^ORCID,Morison Ian M.,Shinawi Marwan^ORCID,Willis Daniel N.^ORCID,Robertson Stephen P.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/s41431-020-00718-4.pdf

Reference29 articles.

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3. Pettenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet. 1986;74:143–54.

4. DeBaun MR, Siegel MJ, Choyke PL. Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome. J Pediatrics. 1998;132:401–4.

5. Brioude F, Kalish JM, Mussa A, Foster AC, Bliek J, Ferrero GB, et al. Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement. Nat Rev Endocrinol. 2018;14:229–49.

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