(Q73093961)

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A novel mutation detected by temporal temperature gradient gel electrophoresis led to the confirmative prenatal diagnosis of a Hispanic CF family

scientific article published on 01 October 2000

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

A novel mutation detected by temporal temperature gradient gel electrophoresis led to the confirmative prenatal diagnosis of a Hispanic CF family (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

L J Wong

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J Wang

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

M Woo

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

E Hsu

4

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1 November 2019

C M Bowman

5

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1 November 2019

publication date

1 October 2000

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Prenatal Diagnosis

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

20

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1 November 2019

10

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1 November 2019

807-810

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1 November 2019

DNA sequence analysis of the KM19 locus linked to cystic fibrosis. Design of new oligonucleotides to remove non-specific PCR products

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Mutation analyses of KRAS exon 1 comparing three different techniques: temporal temperature gradient electrophoresis, constant denaturant capillary electrophoresis and allele specific polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Resolution of DNA linkage discrepancies through analysis of a VNTR locus in a family study of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

High heterogeneity for cystic fibrosis in Spanish families: 75 mutations account for 90% of chromosomes

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Population-specific screening by mutation analysis for diseases frequent in Ashkenazi Jews

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR gene

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

A novel mutation in the CFTR gene correlates with severe clinical phenotype in seven Hispanic patients

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Temperature sweep gel electrophoresis: a simple method to detect point mutations

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Cystic fibrosis: genotypic and phenotypic variations

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200010%2920%3A10%3C807%3A%3AAID-PD929%3E3.0.CO%3B2-A

21 January 2018

Identifiers

10.1002/1097-0223(200010)20:10<807::AID-PD929>3.0.CO;2-A

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11038458%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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