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Search on : VARELLA-GARCIA, MARILEILA [Author]
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 Rosa, Rafael Fabiano Machado et al. Anterior laryngeal membrane and 22q11 deletion syndrome. Braz. j. otorhinolaryngol. (Impr.), Aug 2011, vol.77, no.4, p.540-540. ISSN 1808-8694
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 Rosa, Rafael Fabiano Machado et al. Screening for 22q11 deletion syndrome among patients with congenital heart defects. Sao Paulo Med. J., 2014, vol.132, no.2, p.125-126. ISSN 1516-3180
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 Rosa, Rafael Fabiano Machado et al. Síndrome de deleção 22q11 e cardiopatias congênitas complexas. Rev. Assoc. Med. Bras., Fev 2011, vol.57, no.1, p.62-65. ISSN 0104-4230


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 Koshiyama, Dayane Bohn et al. Síndrome de deleção 22q11.2: importância da avaliação clínica e técnica de FISH. Rev. Assoc. Med. Bras., 2009, vol.55, no.4, p.442-446. ISSN 0104-4230


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 Varella-Garcia, Marileila and Taddei, Valdir Antonio Citogenética de Quirópteros: métodos e aplicações. Rev. Bras. Zool., 1989, vol.6, no.2, p.297-323. ISSN 0101-8175


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 Bellini, Marilanda Ferreira, Silva, Ana Elizabete and Varella-Garcia, Marileila Genomic imbalances in esophageal squamous cell carcinoma identified by molecular cytogenetic techniques. Genet. Mol. Biol., 2010, vol.33, no.2, p.205-213. ISSN 1415-4757
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 Fett-Conte, Agnes C. et al. Atypical chromosome abnormalities in acute myeloid leukemia type M4. Genet. Mol. Biol., 2007, vol.30, no.1, p.6-9. ISSN 1415-4757
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 Varella-Garcia, Marileila. Assessing residual leukemia through fluorescence in situ hybridization. Genet. Mol. Biol., Sept 1998, vol.21, no.3. ISSN 1415-4757
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  Interphase cytogenetics using fluorescence in situ hybridization: an overview of its application to diffuse and solid tissue. . Braz. J. Genet., Mar 1997, vol.20, no.1. ISSN 0100-8455


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 Silva, Ana Elizabete et al. Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder. Arq. Neuro-Psiquiatr., June 2002, vol.60, no.2A, p.290-294. ISSN 0004-282X


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