(Q53175073)

English

A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome.

scientific article published on 9 April 2012

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scholarly article

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome. (English)

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

1

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

author name string

Timothy E Lotze

2

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

Carlos Bacino

3

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

Sau-Wai Cheung

4

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

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publication date

9 April 2012

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

American Journal of Medical Genetics

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

158A

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

1962-1966

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

8

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Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Characterization of mouse UDP-glucose pyrophosphatase, a Nudix hydrolase encoded by the Nudt14 gene

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Expression profile of MTA1 in adult mouse tissues

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Delineation of 14q32.3 deletion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Terminal deletion (14)(q32.3): a new case

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Further delineation of the chromosome 14q terminal deletion syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

The ring 14 syndrome: Clinical and molecular definition

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35289

21 January 2018

Identifiers

10.1002/AJMG.A.35289

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

1 reference

Europe PubMed Central

12 May 2018

http://europepmc.org/abstract/MED/22488736

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