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	1.	Number of rare germline CNVs and TP53 mutation types. [electronic resource] by Silva, Amanda G Achatz, Isabel Maria W Krepischi, Ana Cv Pearson, Peter L Rosenberg, Carla Producer: 20130621 In: Orphanet journal of rare diseases vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability. [electronic resource] by Malvezzi, João Vm H Magalhaes, Ingrid S Costa, Silvia Otto, Paulo A Rosenberg, Carla Bertola, Debora R Lm Fernandes, Walter Vianna-Morgante, Angela M Krepischi, Ana Cv Publication details: Human genome variation 2018 In: Human genome variation vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases. [electronic resource] by Carneiro, Thaise Nr Krepischi, Ana Cv Costa, Silvia S Tojal da Silva, Israel Vianna-Morgante, Angela M Valieris, Renan Ezquina, Suzana Am Bertola, Debora R Otto, Paulo A Rosenberg, Carla Publication details: The application of clinical genetics 2018 In: The application of clinical genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Co-expression network of neural-differentiation genes shows specific pattern in schizophrenia. [electronic resource] by Maschietto, Mariana Tahira, Ana C Puga, Renato Lima, Leandro Mariani, Daniel Paulsen, Bruna da Silveira Belmonte-de-Abreu, Paulo Vieira, Henrique Krepischi, Ana Cv Carraro, Dirce M Palha, Joana A Rehen, Stevens Brentani, Helena Producer: 20160129 In: BMC medical genomics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes. [electronic resource] by Correa, Fernanda A Jorge, Alexander Al Nakaguma, Marilena Canton, Ana Pm Costa, Silvia S Funari, Mariana F Lerario, Antonio M Franca, Marcela M Carvalho, Luciani R Krepischi, Ana Cv Arnhold, Ivo Jp Rosenberg, Carla Mendonca, Berenice B Producer: 20190913 In: Clinical endocrinology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Germline DNA copy number variation in familial and early-onset breast cancer. [electronic resource] by Krepischi, Ana Cv Achatz, Maria Isabel W Santos, Erika Mm Costa, Silvia S Lisboa, Bianca Cg Brentani, Helena Santos, Tiago M Gonçalves, Amanda Nóbrega, Amanda F Pearson, Peter L Vianna-Morgante, Angela M Carraro, Dirce M Brentani, Ricardo R Rosenberg, Carla Producer: 20130207 In: Breast cancer research : BCR vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)