(Q51916075)

17 April 2018

title

Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation. (English)

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17 April 2018

author name string

Pascale Saugier-Veber

1

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17 April 2018

Alice Goldenberg

2

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17 April 2018

Valérie Drouin-Garraud

3

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17 April 2018

Céline de La Rochebrochard

4

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17 April 2018

Valérie Layet

5

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17 April 2018

Nathalie Drouot

6

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17 April 2018

Nathalie Le Meur

7

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17 April 2018

Brigitte Gilbert-Du-Ssardier

8

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17 April 2018

Géraldine Joly-Hélas

9

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17 April 2018

Hélène Moirot

10

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17 April 2018

Annick Rossi

11

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17 April 2018

Mario Tosi

12

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17 April 2018

Thierry Frébourg

13

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17 April 2018

publication date

14 June 2006

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17 April 2018

European Journal of Human Genetics

published in

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17 April 2018

volume

14

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17 April 2018

page(s)

1009-1017

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17 April 2018

issue

9

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17 April 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201661

exact match

0 references

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Estimate of prevalence of proximal 15q duplication syndrome

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inferred from DOI database lookup

7 January 2021

based on heuristic

Significant contribution of germline BRCA2 rearrangements in male breast cancer families

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201661

1 reference

17 April 2018

PubMed ID

16773131

1 reference

17 April 2018