Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature-Reference-Cited by-同舟云学术

Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature

Published:2019-02-26 Issue:7 Volume:27 Page:1061-1071
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Hauer Nadine N.,Popp Bernt^ORCID,Taher Leila,Vogl Carina,Dhandapany Perundurai S.,Büttner Christian,Uebe Steffen,Sticht Heinrich,Ferrazzi Fulvia^ORCID,Ekici Arif B.^ORCID,De Luca Alessandro,Klinger Patrizia,Kraus Cornelia,Zweier Christiane,Wiesener Antje,Jamra Rami Abou^ORCID,Kunstmann Erdmute,Rauch Anita^ORCID,Wieczorek Dagmar,Jung Anna-Marie,Rohrer Tilman R.,Zenker Martin,Doerr Helmuth-Guenther,Reis André^ORCID,Thiel Christian T.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s41431-019-0362-0.pdf

Reference50 articles.

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2. Wood AR, Esko T, Yang J, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014;46:1173–86.

3. Marouli E, Graff M, Medina-Gomez C, et al. Rare and low-frequency coding variants alter human adult height. Nature. 2017;542:186–90.

4. Zahnleiter D, Uebe S, Ekici AB, et al. Rare copy number variants are a common cause of short stature. PLoS Genet. 2013;9:e1003365.

5. Hauer NN, Popp B, Schoeller E, et al. Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature. Genet Med. 2018;20;630–8.

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