Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay (Q33389877)

26 July 2017

title

Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay (English)

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26 July 2017

Taoyun Ji

1

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26 July 2017

Ye Wu

2

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26 July 2017

Huifang Wang

3

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26 July 2017

Jingmin Wang

4

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26 July 2017

Yuwu Jiang

5

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26 July 2017

publication date

3 June 2010

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Journal of Human Genetics

26 July 2017

published in

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26 July 2017

volume

55

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26 July 2017

issue

8

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26 July 2017

page(s)

486-489

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An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

26 July 2017

cites work

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https://api.crossref.org/works/10.1038%2FJHG.2010.51

The 11q terminal deletion disorder: a prospective study of 110 cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Deletion of (11)(q24.2) in a mother and daughter with similar phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Mice deficient in nervous system-specific carbohydrate epitope HNK-1 exhibit impaired synaptic plasticity and spatial learning

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Cloning and chromosomal localization of the human BARX2 homeobox protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

7 January 2021

Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

7 January 2021

Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

7 January 2021

Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.51

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.51

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26 July 2017

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