In the heart of Brazil: clinical evaluation and etiological characterization of mentally retarded semi-institutionalized patients in central-western of Brazil (2009)
- Authors:
- USP affiliated authors: MAZZUCATTO, LUIZ FERNANDO - FMRP ; PINA NETO, JOÃO MONTEIRO DE - FMRP
- Unidade: FMRP
- Subjects: RETARDO MENTAL (ETIOLOGIA); GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: [Mata de São João, BA]
- Date published: 2009
- Source:
- Título do periódico: Abstract
- Conference titles: International Workshop on Fragile X an X- Linked Mental Retardation
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ABNT
LOURENÇO, Charles Marques; RODRIGUEZ, Viviana; MAZZUCATTO, Luiz Fernando; PINA NETO, João Monteiro de. In the heart of Brazil: clinical evaluation and etiological characterization of mentally retarded semi-institutionalized patients in central-western of Brazil. Anais.. [Mata de São João, BA]: [s.n.], 2009. -
APA
Lourenço, C. M., Rodriguez, V., Mazzucatto, L. F., & Pina Neto, J. M. de. (2009). In the heart of Brazil: clinical evaluation and etiological characterization of mentally retarded semi-institutionalized patients in central-western of Brazil. In Abstract. [Mata de São João, BA]. -
NLM
Lourenço CM, Rodriguez V, Mazzucatto LF, Pina Neto JM de. In the heart of Brazil: clinical evaluation and etiological characterization of mentally retarded semi-institutionalized patients in central-western of Brazil. Abstract. 2009 ; -
Vancouver
Lourenço CM, Rodriguez V, Mazzucatto LF, Pina Neto JM de. In the heart of Brazil: clinical evaluation and etiological characterization of mentally retarded semi-institutionalized patients in central-western of Brazil. Abstract. 2009 ; - Síndrome da microdeleção 1p36: avaliação clínico-laboratorial revela a existência de um fenótipo só
- Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto
- Cytogenetic analysis of individuals affected by mental retardation in APAE of the city of Limeira-SP
- De novo complex chromosome rearrangement: a study of two patients
- Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men
- Efeito da idade na frequência de aberrações cromossômicas em espermatozóides humanos
- Sinais clínicos associados a rearranjo cromossômico complexo 2P, 7P, 13Q
- Cytogenetics studies in mild mental retardation
- Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype
- Associação entre citogenética clássica e molecular na descrição de um rearranjo complexo envolvendo os cromossomos 1,2,3,4 e 12
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