(Q34287832)

English

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

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

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

1 reference

Europe PubMed Central

1 August 2017

Miller–Dieker lissencephaly syndrome

0 references

Contiguous gene syndrome

1 reference

based on heuristic

inferred from title

author name string

D H Ledbetter

1

1 reference

Europe PubMed Central

1 August 2017

S A Ledbetter

2

1 reference

Europe PubMed Central

1 August 2017

P vanTuinen

3

1 reference

Europe PubMed Central

1 August 2017

K M Summers

4

1 reference

Europe PubMed Central

1 August 2017

T J Robinson

5

1 reference

Europe PubMed Central

1 August 2017

Y Nakamura

6

1 reference

Europe PubMed Central

1 August 2017

R Wolff

7

1 reference

Europe PubMed Central

1 August 2017

R White

8

1 reference

Europe PubMed Central

1 August 2017

D F Barker

9

1 reference

Europe PubMed Central

1 August 2017

M R Wallace

10

1 reference

Europe PubMed Central

1 August 2017

language of work or name

0 references

publication date

1 July 1989

1 reference

Europe PubMed Central

1 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

1 August 2017

86

1 reference

Europe PubMed Central

1 August 2017

5136-5140

1 reference

Europe PubMed Central

1 August 2017

13

1 reference

Europe PubMed Central

1 August 2017

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

A highly polymorphic region 3' to the human type II collagen gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Comparative chromosome mapping of a conserved homoeo box region in mouse and human

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Hypervariable 'minisatellite' regions in human DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Developmental aspects of lissencephaly and the lissencephaly syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Genetic analysis of NF1: identification of close flanking markers on chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Variable number of tandem repeat (VNTR) markers for human gene mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

A new hypervariable marker for the human alpha-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

A mapped set of DNA markers for human chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

6 July 2018

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

28 October 2018

New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

28 October 2018

Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297572

28 October 2018

Spasmodic, a mutation on chromosome 11 in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/2740347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of hypervariable minisatellites in the proterminal regions of human autosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2740347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic analysis of extinction: Trans-dominant loci regulate expression of liver-specific traits in hepatoma hybrid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2740347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.86.13.5136

1 reference

Europe PubMed Central

1 August 2017

1989PNAS...86.5136L

0 references

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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