Pure 21q22.3 deletion identified in a patient with mild phenotypic features

Sgardioli, Ilaria Cristina; Copelli, Matheus de Melo; Lustosa-Mendes, Elaine; Vieira, Tarsis Paiva; Gil-da-Silva-Lopes, Vera Lucia

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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Pure 21q22.3 deletion identified in a patient with mild phenotypic features

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Author(s):	Sgardioli, Ilaria Cristina ^[1] ; Copelli, Matheus de Melo ^[1] ; Lustosa-Mendes, Elaine ^[1] ; Vieira, Tarsis Paiva ^[1] ; Gil-da-Silva-Lopes, Vera Lucia ^[1] Total Authors: 5
Affiliation:	^[1] Univ Estadual Campinas, Fac Med Sci, Dept Med Genet, Campinas, SP - Brazil Total Affiliations: 1
Document type:	Journal article
Source:	CONGENITAL ANOMALIES; v. 58, n. 5, p. 178-180, SEP 2018.
Web of Science Citations:	0
Abstract


FAPESP's process:	12/51799-6 - Consolidation of a multicentric strategy in genetics for database and diagnostic on orofacial clefts
Grantee:	Vera Lúcia Gil da Silva Lopes
Support Opportunities:	Research Grants - Research in Public Policies for the National Health Care System (PP-SUS)

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