(Q55670707)

2

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Marina Murdolo

3

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Serena Lattante

4

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Domenica Battaglia

5

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Chiara Stefanini

6

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Eugenio Mercuri

7

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Pietro Chiurazzi

8

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Giovanni Neri

9

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Giuseppe Marangi

https://scigraph.springernature.com/pub.10.1038/ng.2257

10

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language of work or name

English

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publication date

29 April 2012

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published in

Nature Genetics

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volume

44

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issue

6

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page(s)

636-8

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exact match

0 references

cites work

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Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

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Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

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Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome.

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17q21.31 microdeletion syndrome: further expanding the clinical phenotype.

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Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation

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Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

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