Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.

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Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability

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P2860

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.

Monogenic causes of X-linked mental retardation.

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10.1159/000334289

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