Cryptic genomic imbalances as a cause of syndromic X-linked mental retardation (2005)
- Authors:
- USP affiliated authors: MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB
- Unidade: IB
- Subjects: RETARDO MENTAL; CITOGENÉTICA; GENÓTIPOS
- Language: Inglês
- Imprenta:
- Publisher place: Williamsburg
- Date published: 2005
- Source:
- Título do periódico: Abstract
- Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation
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ABNT
VIANNA-MORGANTE, Angela Maria; KNIJNENBURG, Jeroen; OTTO, Paulo Alberto; et al. Cryptic genomic imbalances as a cause of syndromic X-linked mental retardation. Anais.. Williamsburg: [s.n.], 2005. -
APA
Vianna-Morgante, A. M., Knijnenburg, J., Otto, P. A., Krepischi-Santos, A. C. V., Nascimento, R. M. P., & Rosenberg, C. (2005). Cryptic genomic imbalances as a cause of syndromic X-linked mental retardation. In Abstract. Williamsburg. -
NLM
Vianna-Morgante AM, Knijnenburg J, Otto PA, Krepischi-Santos ACV, Nascimento RMP, Rosenberg C. Cryptic genomic imbalances as a cause of syndromic X-linked mental retardation. Abstract. 2005 ; -
Vancouver
Vianna-Morgante AM, Knijnenburg J, Otto PA, Krepischi-Santos ACV, Nascimento RMP, Rosenberg C. Cryptic genomic imbalances as a cause of syndromic X-linked mental retardation. Abstract. 2005 ; - Notes on the population genetics of fragile x syndrome
- Síndrome de Saethre-Chotzen associada a deleção do braço curto do cromossomo 7
- Mutação do gene UBE2A (de enzima conjugadora de ubiquitina) causa nova síndrome de retardo mental de herança ligada ao X
- Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents
- Inativacao do x fragil e a manifestacao do retardado mental nas heterozigotas
- Effect of x inactivation on fragile x frequency and mental retardation
- Replication timing of homologous 'alfa'-satelite DNA in Roberts syndrome
- Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1
- Evaluating the contribution of X-chromosome mutations to mental retardation based on the pattern of X inactivation in mothers of affected boys
- Como diagnosticar possiveis heterozigotas que manifestam baixas frequencias de fra (x)?
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