(Q48332931)

10 February 2018

title

Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation (English)

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10 February 2018

author

Jozef Gécz

3

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10 February 2018

Wei Chen

object named as

Wei Chen

1

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author name string

Lars R Jensen

2

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Jean-Pierre Fryns

4

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Claude Moraine

5

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Arjan de Brouwer

6

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Jamel Chelly

7

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Bettina Moser

8

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10 February 2018

H Hilger Ropers

9

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Andreas W Kuss

10

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10 February 2018

publication date

20 December 2006

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10 February 2018

European Journal of Human Genetics

published in

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10 February 2018

volume

15

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10 February 2018

issue

3

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10 February 2018

page(s)

375-378

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10 February 2018

The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

MicroRNAs modulate hematopoietic lineage differentiation

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

A pancreatic islet-specific microRNA regulates insulin secretion

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

MicroRNAs regulate brain morphogenesis in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

Five years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study reporting 95% of the activity in France.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

Screening of the ARX gene in 682 retarded males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

The epidemiology of mental retardation: challenges and opportunities in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

MicroRNAs: genomics, biogenesis, mechanism, and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

Identification of hundreds of conserved and nonconserved human microRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

MicroRNA maturation: stepwise processing and subcellular localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201758

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201758

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10 February 2018

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10 February 2018