Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

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Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

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http://www.wikidata.org/entity/Q41580601

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2011 nî lūn-bûn

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2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

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2011年论文

@zh

2011年论文

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Prenatally diagnosed submicros ...... 1.32 without phenotypic effect

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Item

label

Prenatally diagnosed submicros ...... 1.32 without phenotypic effect

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prefLabel

Prenatally diagnosed submicros ...... 1.32 without phenotypic effect

@en

P1476

Prenatally diagnosed submicros ...... 1.32 without phenotypic effect

@en

P2093

Carla Ma Verboven-Peerden

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Diane Van Opstal

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Gerda Ag Looye-Bruinsma

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Gretel Oudesluijs

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Marjan Boter

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Robert-Jan H Galjaard

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P2860

Monosomy 18p

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.

Psychiatric syndromes in individuals with chromosome 18 abnormalities.

18p monosomy with midline defects and a de novo satellite identified by FISH.

Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.

Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.

18p trisomy: a case of direct 18p duplication characterized by molecular cytogenetic analysis.

P2888

1755-8166-4-27

P304

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P31

scholarly article

P356

10.1186/1755-8166-4-27

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P433

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P478

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P50

Malgorzata Srebniak

P577

2011-12-02T00:00:00Z

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P5875

51848824

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P6179

1004723468

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P698

22136596

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P932

3287247

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