(Q38469378)

English

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

scientific article published on 06 March 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Herman E Wyandt

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sung Han Shim

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Hon Fong L Mark

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Xin Li Huang

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Jeff M Milunsky

5

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Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

6 March 2006

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Europe PubMed Central

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3 September 2017

Experimental and Molecular Pathology

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Europe PubMed Central

PubMed publication ID

3 September 2017

80

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Europe PubMed Central

PubMed publication ID

3 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

262-266

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

High resolution comparative genomic hybridisation in clinical cytogenetics

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Molecular genetics of Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2005.12.008

7 January 2021

Identifiers

10.1016/J.YEXMP.2005.12.008

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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