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 APA Style APA-ALL Style AAA 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., Ribeiro-Bicudo, L.A., Fitzpatrick, D., Guion-Almeida, M.L.& 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.https://doi.org/10.1055/s-0039-3402047

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