author-photo

Claudia Danielli Pereira Bertolacini

University of São Paulo

4

Papers

98

Citations

Citation Trend

Filter By

Papers (4) Sort By

Journal Conference Others

Clinical findings in patients with GLI2 mutations – phenotypic variability

2012 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (43)
A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis.

2011 Clinical Dysmorphology
Show All
- Source
- Cite
- Save
Citations (1)
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients.

2010 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (47)
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: Exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes

2009 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (7)