(Q48680637)

English

Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13.

scientific article published in August 1991

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scholarly article

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13. (English)

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

0 references

author name string

J F De Rijk-van Andel

1

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

C E Catsman-Berrevoets

2

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

D J Halley

3

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

E Wesby-van Swaay

4

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

M F Niermeijer

5

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

B A Oostra

6

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

publication date

1 August 1991

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

87

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

4

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

509-510

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

https://scigraph.springernature.com/pub.10.1007/bf00197179

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neurogenetics of lissencephaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A hypervariable RFLP on chromosome 17p13 is defined by an arbitrary single copy probe p144-D6 [HGM9 No. D17S34]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EEG and evoked potentials in a series of 21 patients with lissencephaly type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic features and clinical signs of 21 patients with lissencephaly type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00197179

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

1 reference

Europe PubMed Central

14 February 2018

http://europepmc.org/abstract/MED/1879837

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