(Q35196840)

7 August 2017

title

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization (English)

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Miller–Dieker lissencephaly syndrome

7 August 2017

main subject

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3

W B Dobyns

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7 August 2017

A Kuwano

1

1 reference

7 August 2017

S A Ledbetter

series ordinal

2

1 reference

7 August 2017

B S Emanuel

series ordinal

4

1 reference

7 August 2017

D H Ledbetter

series ordinal

5

1 reference

7 August 2017

language of work or name

English

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publication date

1 October 1991

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

49

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7 August 2017

issue

4

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7 August 2017

page(s)

707-714

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describes a project that uses

7 August 2017

in situ hybridization

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Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

A highly polymorphic locus in human DNA revealed by cosmid-derived probes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Detection of the Philadelphia chromosome in interphase nuclei

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Clinical and molecular diagnosis of Miller-Dieker syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683159

A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes

26 September 2018

1 reference

12 December 2020

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

1 reference

12 December 2020

Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization

1 reference

12 December 2020

An improved method for G-banding chromosomes after in situ hybridization

1 reference

12 December 2020

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

1 reference

12 December 2020

Identifiers

PMC publication ID

1683159

1 reference

7 August 2017

1 reference