(Q38289951)

1 September 2017

title

Low-density DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathy (English)

1 reference

1 September 2017

Stephan Waldmüller

1

1 reference

1 September 2017

Petra Freund

2

1 reference

1 September 2017

Simon Mauch

3

1 reference

1 September 2017

Roland Toder

4

1 reference

1 September 2017

Hans-Peter Vosberg

5

1 reference

1 September 2017

publication date

1 May 2002

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1 September 2017

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1 September 2017

volume

19

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1 September 2017

issue

5

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1 September 2017

page(s)

560-569

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Rapid p53 sequence analysis in primary lung cancer using an oligonucleotide probe array

1 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Exploring the new world of the genome with DNA microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Polymorphic human cytochrome P450 enzymes: an opportunity for individualized drug treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

A chemiluminescent assay for quantitation of β-galactosidase in the femtogram range: Application to quantitation of β-galactosidase in lacZ-transfected cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Extensive polymorphisms observed in HIV-1 clade B protease gene using high-density oligonucleotide arrays.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Cardiovascular risks to young persons on the athletic field.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

DNA chips: an array of possibilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Prognosis in hypertrophic cardiomyopathy: role of age and clinical, electrocardiographic and hemodynamic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Alteration of the relative stability of dA-dT and dG-dC base pairs in DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

A sequencing method based on real-time pyrophosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

The Genetic Basis for Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

The management of hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10074

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.10074

1 reference

release_5rcruqwxk5a6rhrrzxpiwnblly

1 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/5rcruqwxk5a6rhrrzxpiwnblly

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference