Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome. - Wikidata - wikimedia - TriplyDB

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome.

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome.

http://www.wikidata.org/entity/Q35177841

about

A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies.Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report.

P2860

Q37712903-A4A5D498-8011-4D39-8015-97631BC47BD3 Q40834169-CCEB132F-2D62-48DE-A4D2-A20F9AA53427

P2860

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome.

http://www.wikidata.org/entity/Q35177841

description

2015 nî lūn-bûn

@nan

2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@ast

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@en

type

label

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@ast

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@en

prefLabel

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@ast

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@en

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P356

S13039-015-0111-1

P1433

Molecular Cytogenetics

P1476

Partial trisomy 2q33.3-q37.3 i ...... neocentric marker chromosome.

@en

P2093

Baoheng Gui

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

Chen Chen

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

Desheng Liang

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

Guizhi Tang

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

Jiazhen Chang

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

Lingqian Wu

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

Ruiyu Ma

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

Ruolan Guo

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

Yan Xia

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

Yanghui Zhang

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

P2860

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35).

Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome.

Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.

Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.

Chromosome 2q duplications: case report of a de novo interstitial duplication and review of the literature.

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.

Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution

A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

A female infant with duplication of chromosome 2q33 to 2q37.3.

P2888

s13039-015-0111-1

P304

10

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P31

scholarly article

P356

10.1186/S13039-015-0111-1

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P478

8

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2015-02-06T00:00:00Z

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272389237

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P6179

1037228111

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P698

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P932

4359772

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