(Q35755758)

10 August 2017

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title

MLPA and MAPH: new techniques for detection of gene deletions (English)

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10 August 2017

Loryn N Sellner

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10 August 2017

Graham R Taylor

series ordinal

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10 August 2017

language of work or name

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1 May 2004

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10 August 2017

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10 August 2017

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10 August 2017

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10 August 2017

page(s)

413-419

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Measurement of locus copy number by hybridisation with amplifiable probes

10 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

The development and clinical use of trastuzumab (Herceptin).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

High throughput screening of human subtelomeric DNA for copy number changes using multiplex amplifiable probe hybridisation (MAPH)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Correlation of allelic losses and clinicopathological factors in 504 primary breast cancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Prognostic impact of multiple allelic losses on metastatic recurrence in hepatocellular carcinoma after curative resection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20035

7 January 2021

Identifiers

DOI

10.1002/HUMU.20035

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10 August 2017

1 reference