(Q46901571)

26 December 2017

title

The hyper-IgE syndrome is not caused by a microdeletion syndrome (English)

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26 December 2017

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11

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26 December 2017

Stephan Ehl

7

object named as

Stephan Ehl

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26 December 2017

Jennifer M Puck

10

object named as

Jennifer M Puck

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26 December 2017

Bodo Grimbacher

12

object named as

Bodo Grimbacher

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26 December 2017

author name string

Dietmar Pfeifer

1

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26 December 2017

Cristina Woellner

2

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26 December 2017

Astrid Petersen

3

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26 December 2017

Maria Cristina Pietrogrande

4

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26 December 2017

Josè Luis Franco

5

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26 December 2017

Mehdi Yeganeh

6

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26 December 2017

Nuria Matamoros

8

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26 December 2017

Eli Sprecher

9

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26 December 2017

language of work or name

English

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publication date

14 November 2007

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26 December 2017

published in

Immunogenetics

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26 December 2017

volume

59

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26 December 2017

issue

12

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26 December 2017

page(s)

913-926

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26 December 2017

https://scigraph.springernature.com/pub.10.1007/s00251-007-0257-z

exact match

0 references

cites work

Analphoid marker chromosome in a patient with hyper-IgE syndrome, autism, and mild mental retardation.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00251-007-0257-Z

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00251-007-0257-Z

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

21 January 2018

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity

1 reference

12 December 2020

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

1 reference

12 December 2020

Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum

1 reference

12 December 2020

1 reference

12 December 2020

Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.

1 reference

12 December 2020

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

1 reference

12 December 2020

Global variation in copy number in the human genome

1 reference

12 December 2020

Detection of large-scale variation in the human genome

1 reference

12 December 2020

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

1 reference

12 December 2020

STAT3 mutations in the hyper-IgE syndrome

1 reference

12 December 2020

Quantitative linkage genome scan for atopy in a large collection of Caucasian families

1 reference

12 December 2020

High-resolution analysis of DNA copy number using oligonucleotide microarrays

1 reference

12 December 2020

DiGeorge syndrome and pharyngeal apparatus development

1 reference

12 December 2020

Genetic linkage of hyper-IgE syndrome to chromosome 4.

1 reference

12 December 2020

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

1 reference

12 December 2020

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

1 reference

12 December 2020

10.1007/S00251-007-0257-Z

Identifiers

DOI

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26 December 2017

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26 December 2017