Publications by authors named "Ingrid Cristian"

8Publications

Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?

Am J Med Genet A 2017 Jun 25;173(6):1593-1600. Epub 2017 Apr 25.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.38241DOI Listing
June 2017

Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.

J Med Genet 2015 Jun 20;52(6):413-21. Epub 2015 Mar 20.

Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1136/jmedgenet-2015-103018DOI Listing
June 2015

Ocular findings and treatment of a young boy with Coats’ plus.

Ophthalmic Surg Lasers Imaging Retina 2014 Sep-Oct;45(5):462-5

Weill Cornell Medical College, New York, New York, USA.

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http://www.healio.com/doiresolver?doi=10.3928/23258160-20140
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http://dx.doi.org/10.3928/23258160-20140827-02DOI Listing
October 2015