(Q48501399)

12 February 2018

title

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. (English)

1 reference

12 February 2018

6q terminal deletion syndrome

main subject

1 reference

1

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12 February 2018

Marco Fichera

3

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Ornella Galesi

6

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Sebastiano Antonino Musumeci

10

1 reference

12 February 2018

Corrado Romano

11

1 reference

12 February 2018

Carmelo Amato

object named as

Carmelo Amato

9

0 references

Lucia Castiglia

object named as

Lucia Castiglia

5

0 references

Federico Zara

object named as

Federico Zara

14

0 references

author name string

Pasquale Striano

2

1 reference

12 February 2018

Roberto Gaggero

4

1 reference

12 February 2018

Michela Malacarne

7

1 reference

12 February 2018

Mauro Pierluigi

8

1 reference

12 February 2018

Silvia Majore

12

1 reference

12 February 2018

Paola Grammatico

13

1 reference

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Salvatore Striano

15

1 reference

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Francesca Faravelli

16

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publication date

1 May 2006

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12 February 2018

published in

Epilepsia

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12 February 2018

volume

47

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12 February 2018

issue

5

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12 February 2018

page(s)

830-838

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12 February 2018

New insights into the phenotypes of 6q deletions

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Subtle chromosomal rearrangements in children with unexplained mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

6q subtelomeric deletion: is there a recognizable syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Calibration of 6q subtelomere deletions to define genotype/phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Colpocephaly and Gilles de la Tourette's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Colpocephaly: clinical, radiologic, and pathogenetic aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Commissural connections of human superior colliculus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Transient neonatal diabetes, a disorder of imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

Chromosome abnormalities and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

An imprinted locus associated with transient neonatal diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2006.00522.X

10.1111/J.1528-1167.2006.00522.X

21 January 2018

Identifiers

DOI

1 reference

12 February 2018

1 reference

12 February 2018