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	1.	Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH. [electronic resource] by Barbaro, Michela Soardi, Fernanda C de Mello, Maricilda Palandi Wedell, Anna Lajic, Svetlana Producer: 20120823 In: Clinical endocrinology vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Iron-responsive genes of Phanerochaete chrysosporium isolated by differential display reverse transcription polymerase chain reaction. [electronic resource] by Assmann, Eliana Maria Ottoboni, Laura Maria Mariscal Ferraz, André Rodríguez, Jaime De Mello, Maricilda Palandi Producer: 20031110 In: Environmental microbiology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Iron-regulated proteins in Phanerochaete chrysosporium and Lentinula edodes: differential analysis by sodium dodecyl sulfate polyacrylamide gel electrophoresis and two-dimensional polyacrylamide gel electrophoresis profiles. [electronic resource] by Hernández-Macedo, Maria L Ferraz, André Rodríguez, Jaime Ottoboni, Laura M M De Mello, Maricilda Palandi Producer: 20021008 In: Electrophoresis vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia. [electronic resource] by Barbaro, Michela Soardi, Fernanda C Östberg, Linus J Persson, Bengt de Mello, Maricilda Palandi Wedell, Anna Lajic, Svetlana Producer: 20150903 In: Clinical endocrinology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutation update for the NR5A1 gene involved in DSD and infertility. [electronic resource] by Fabbri-Scallet, Helena de Sousa, Lizandra Maia Maciel-Guerra, Andréa Trevas Guerra-Júnior, Gil de Mello, Maricilda Palandi Producer: 20210519 In: Human mutation vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases. [electronic resource] by Rocha, Vanessa Brito Campoy Guerra-Júnior, Gil Marques-de-Faria, Antonia Paula de Mello, Maricilda Palandi Maciel-Guerra, Andréa Trevas Producer: 20120123 In: Fertility and sterility vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Q289P mutation in FGFR2 gene causes Saethre-Chotzen syndrome: some considerations about familial heterogeneity. [electronic resource] by Freitas, Erika Cristina Lopes Burrone de Nascimento, Sandra Regina Dantas de Mello, Maricilda Palandi Gil-da-Silva-Lopes, Vera Lúcia Producer: 20060511 In: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Severe forms of partial androgen insensitivity syndrome due to p.L830F novel mutation in androgen receptor gene in a Brazilian family. [electronic resource] by Petroli, Reginaldo J Maciel-Guerra, Andréa T Soardi, Fernanda C de Calais, Flávia L Guerra-Junior, Gil de Mello, Maricilda Palandi Producer: 20110714 In: BMC research notes vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Three new Brazilian cases of 17α-hydroxylase deficiency: clinical, molecular, hormonal, and treatment features. [electronic resource] by Breder, Ikaro Soares Santos Garmes, Heraldo Mendes Mazzola, Tais Nitsch Maciel-Guerra, Andrea Trevas de Mello, Maricilda Palandi Guerra-Júnior, Gil Producer: 20181127 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A study of splicing mutations in disorders of sex development. [electronic resource] by de Calais, Flavia Leme Smith, Lindsay D Raponi, Michela Maciel-Guerra, Andréa Trevas Guerra-Junior, Gil de Mello, Maricilda Palandi Baralle, Diana Producer: 20190709 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene. [electronic resource] by Coeli, Fernanda Borchers Ferraz, Lúcio Fábio Caldas Lemos-Marini, Sofia H V de Rigatto, Sumara Zuanazi Pinto Belangero, Vera Maria Santoro de-Mello, Maricilda Palandi Producer: 20091007 In: Arquivos brasileiros de endocrinologia e metabologia vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants. [electronic resource] by dos Santos, Ana Paula Andrade, Juliana Gabriel Ribeiro Piveta, Cristiane Santos Cruz de Paulo, Juliana Guerra, Gil de Mello, Maricilda Palandi Maciel-Guerra, Andréa Trevas Producer: 20140408 In: BMC medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets. [electronic resource] by Macedo, Luciana Cosentino de Soardi, Fernanda Caroline Ananias, Nayla Belangero, Vera Maria Santoro Rigatto, Sumara Zuazani Pinto De-Mello, Maricilda Palandi D'Souza-Li, Lília Producer: 20091007 In: Arquivos brasileiros de endocrinologia e metabologia vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males. [electronic resource] by Gabriel Ribeiro de Andrade, Juliana Marques-de-Faria, Antonia Paula Fabbri, Helena Campos de Mello, Maricilda Palandi Guerra-Júnior, Gil Maciel-Guerra, Andréa Trevas Producer: 20150112 In: International journal of endocrinology vol. 2014 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins. [electronic resource] by Esquiaveto-Aun, Adriana Mangue De Mello, Maricilda Palandi Paulino, Maria Fernanda Vanti Macedo Minicucci, Walter José Guerra-Júnior, Gil De Lemos-Marini, Sofia Helena Valente Producer: 20151120 In: Diabetology & metabolic syndrome vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia. [electronic resource] by Prado, Mayara Jorgens de Castro, Simone Martins Kopacek, Cristiane de Mello, Maricilda Palandi Rispoli, Thaiane Grandi, Tarciana da Silva, Cláudia Maria Dornelles Rossetti, Maria Lucia Rosa Producer: 20180621 In: Molecular diagnosis & therapy vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density. [electronic resource] by de Almeida Freire, Patrícia Oliveira de Lemos-Marini, Sofia Helena Valente Maciel-Guerra, Andréa Trevas Morcillo, André Moreno Matias Baptista, Maria Tereza de Mello, Maricilda Palandi Guerra, Gil Producer: 20040702 In: Journal of bone and mineral metabolism vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Promises and pitfalls of whole-exome sequencing exemplified by a nephrotic syndrome family. [electronic resource] by Guaragna, Mara Sanches de Brito Lutaif, Anna Cristina Gervásio de Souza, Marcela Lopes Maciel-Guerra, Andréa Trevas Belangero, Vera Maria Santoro Guerra-Júnior, Gil de Mello, Maricilda Palandi Producer: 20200121 In: Molecular genetics and genomics : MGG vol. 295 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents. [electronic resource] by Della Torre, Osmar Henrique Paes, Lúcia Arisaka Henriques, Taciane Barbosa de Mello, Maricilda Palandi Celeri, Eloisa Helena Rubello Valler Dalgalarrondo, Paulo Guerra-Júnior, Gil Santos-Júnior, Amilton Dos Producer: 20190225 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	New mutation in the myocilin gene segregates with juvenile-onset open-angle glaucoma in a Brazilian family. [electronic resource] by Braghini, Carolina Ayumi Neshich, Izabella Agostinho Pena Neshich, Goran Soardi, Fernanda Caroline de Mello, Maricilda Palandi Costa, Vital Paulino de Vasconcellos, José Paulo Cabral de Melo, Mônica Barbosa Producer: 20130711 In: Gene vol. 523 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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