(Q34386784)

1 August 2017

title

Rearrangements of chromosome 15 in epilepsy (English)

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1 August 2017

Torrisi L

1

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1 August 2017

Sangiorgi E

series ordinal

2

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1 August 2017

Russo L

series ordinal

3

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1 August 2017

Gurrieri F

series ordinal

4

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1 August 2017

publication date

1 January 2001

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American Journal of Medical Genetics Part A

1 August 2017

published in

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1 August 2017

volume

106

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1 August 2017

issue

2

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1 August 2017

page(s)

125-128

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The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

1 August 2017

cites work

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Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

21 January 2018

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Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

21 January 2018

1 reference

Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis.

21 January 2018

1 reference

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

21 January 2018

1 reference

Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome

21 January 2018

1 reference

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

21 January 2018

1 reference

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

21 January 2018

1 reference

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

21 January 2018

1 reference

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

21 January 2018

1 reference

Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay

21 January 2018

1 reference

Intrachromosomal triplication of 15q11-q13.

21 January 2018

1 reference

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.

21 January 2018

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Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AJMG.1570

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1 August 2017

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