Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2

Vendramini-Pittoli, S., Candido-Souza, R.M., Quiezi, R.G., R.M. Zechi-Ceide (Roseli Maria), Kokitsu-Nakata, N.M., Jehee, F.S., Ribeiro-Bicudo, L.A., D.R. Fitzpatrick (David), Guion-Almeida, M.L. and Richieri-Costa, A.

2020

Journal of Pediatric Genetics , Volume 09 - Issue 04 p. 258- 262

Additional Metadata
Persistent URL	doi.org/10.1055/s-0039-3402047, hdl.handle.net/1765/130600
Journal	Journal of Pediatric Genetics
Rights	no subscription
Organisation	Department of Clinical Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Vendramini-Pittoli, S., Candido-Souza, R.M., Quiezi, R.G., Zechi-Ceide, R.M, Kokitsu-Nakata, N.M., Jehee, F.S., … Richieri-Costa, A. (2020). Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2. Journal of Pediatric Genetics, 09(04), 258–262. doi:10.1055/s-0039-3402047

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