Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB. - Wikidata - awgldk - TriplyDB

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

http://www.wikidata.org/entity/Q34691567

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Methylation of Integrin α4 and E-Cadherin Genes in Human Prostate Cancer.

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Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

http://www.wikidata.org/entity/Q34691567

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@ast

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@en

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@nl

type

label

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@ast

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@en

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@nl

prefLabel

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@ast

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@en

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@nl

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Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.

@en

P2093

Chung-Hsing Wang

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Fuu-Jen Tsai

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Huang-Tsung Kuo

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I-Ching Chou

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Siew-Yin Chee

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Wei-De Lin

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Yu-Tzu Chang

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P2860

The molecular basis of Sanfilippo syndrome type B

Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25

Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

Hypothesis for development of a behavioral phenotype in Williams syndrome.

Interstitial deletion of the long arm of chromosome 3: case report, review, and definition of a phenotype.

Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.

Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.

Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.

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7

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scholarly article

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10.7603/S40681-014-0007-0

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4

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2014-08-06T00:00:00Z

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25520920

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4264972

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