Clinical and molecular characterization of a de novo 19p13.3 microdeletion

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Ocular Manifestations of a Novel Proximal 19p13.3 Microdeletion.

P2860

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P2860

Clinical and molecular characterization of a de novo 19p13.3 microdeletion

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http://www.wikidata.org/entity/Q36942065

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

Clinical and molecular characterization of a de novo 19p13.3 microdeletion

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type

Item

label

Clinical and molecular characterization of a de novo 19p13.3 microdeletion

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Clinical and molecular characterization of a de novo 19p13.3 microdeletion

@en

P1476

Clinical and molecular characterization of a de novo 19p13.3 microdeletion

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P2093

Leopoldo Zelante

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Orazio Palumbo

http://www.w3.org/2001/XMLSchema#string

Pietro Palumbo

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Raffaella Stallone

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Teresa Palladino

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P2860

The DNA sequence and biology of human chromosome 19

Identification of a brain-specific APC homologue, APCL, and its interaction with beta-catenin

Cloning, chromosal mapping, and tissue expression of the gene encoding the human Eph-family kinase ligand ephrin-A2

Plk5, a polo box domain-only protein with specific roles in neuron differentiation and glioblastoma suppression

Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features

Novel nucleolar protein, midnolin, is expressed in the mesencephalon during mouse development

Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.

Whole exome sequencing in females with autism implicates novel and candidate genes.

Polo-like kinases: conservation and divergence in their functions and regulation.

Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.

P2888

s13039-016-0252-x

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scholarly article

case report

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10.1186/S13039-016-0252-X

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P478

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Massimo Carella

Maria Pia Leone

P577

2016-05-27T00:00:00Z

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1009246622

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27239227

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P932

4882821

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Clinical and molecular characterization of a de novo 19p13.3 microdeletion

about

P2860

P2860

Clinical and molecular characterization of a de novo 19p13.3 microdeletion

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P6179

P698

P932