Sweeney-Cox syndrome: report of the third patient affected by this new delineated syndrome harboring a novel variant in TWIST1

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Author(s):	Bertola, D. ; Musso, C. M. ; Rocha, K. ; Yamamoto, G. L. ; Passos-Bueno, M. Total Authors: 5
Document type:	Journal article
Source:	European Journal of Human Genetics; v. 27, p. 2-pg., 2019-07-01.

FAPESP's process:	13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center
Grantee:	Mayana Zatz
Support Opportunities:	Research Grants - Research, Innovation and Dissemination Centers - RIDC


FAPESP's process:	15/21783-9 - Analysis of genetic variants in rare osteochondrodysplasias using whole exome sequencing
Grantee:	Débora Romeo Bertola
Support Opportunities:	Regular Research Grants