Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.

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Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

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Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

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Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

@en

Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

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Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

@en

Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

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P1476

Identifying CNVs in 15q11q13 a ...... Detecting Pathogenic Changes.

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P2093

Andréia M Carvalho

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Elvis C Mateo

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Fernanda S Jehee

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Gabrielle S Vianna

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Giovana da C César

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Joziele de S Lima

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Juliana G Giannetti

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Luana C A Ferreira

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Maria Augusta N P Monteiro

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Mariana L Freitas

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P2860

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

Global variation in copy number in the human genome

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Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype.

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.

Epilepsy and chromosomal abnormalities.

Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.

P304

329-336

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P31

scholarly article

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10.1159/000450631

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P478

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P577

2016-11-01T00:00:00Z

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27920636

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5131333

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