(Q51988502)

19 April 2018

title

Characteristic EEG findings in ring 20 syndrome as a diagnostic clue. (English)

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19 April 2018

author name string

Kobayashi K

1

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19 April 2018

Inagaki M

2

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19 April 2018

Sasaki M

3

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19 April 2018

Sugai K

4

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19 April 2018

Ohta S

5

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19 April 2018

Hashimoto T

6

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19 April 2018

publication date

1 October 1998

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19 April 2018

Electroencephalography and Clinical Neurophysiology

published in

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19 April 2018

volume

107

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19 April 2018

issue

4

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19 April 2018

page(s)

258-262

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19 April 2018

Familial ring (20) chromosomal mosaicism

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Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease

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Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20

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Ring chromosome 20 and nonconvulsive status epilepticus. A new epileptic syndrome

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Number 20 ring chromosome: a case with complete seizure control

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Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

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Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability.

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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

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Infantile spasms in down syndrome: A report of 5 cases and review of the literature

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Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3

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Ring 14 chromosome with complex partial seizures: a case report

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7 January 2021

Ring formation of chromosomes nos. 19 and 20

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7 January 2021

10.1016/S0013-4694(98)00069-8

Identifiers

DOI

1 reference

19 April 2018

1 reference

19 April 2018