DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2 (Q57251887)

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4 November 2019

title

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2 (English)

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4 November 2019

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16

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4 November 2019

author name string

Y Müller-Koch

2

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4 November 2019

W Friedl

3

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4 November 2019

G Moeslein

4

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4 November 2019

G Keller

5

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4 November 2019

J Plaschke

6

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4 November 2019

W Ballhausen

7

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4 November 2019

M Gross

8

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4 November 2019

K Baldwin-Jedele

9

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4 November 2019

M Jungck

10

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4 November 2019

E Mangold

11

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4 November 2019

H Vogelsang

12

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4 November 2019

P Lohsea

14

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4 November 2019

J Murken

15

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4 November 2019

E Holinski-Feder

1

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H K Schackert

13

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4 November 2019

publication date

1 January 2001

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4 November 2019

published in

Journal of Proteomics

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4 November 2019

volume

47

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4 November 2019

issue

1-2

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4 November 2019

page(s)

21-32

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Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-022X%2800%2900148-2

7 January 2021

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

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7 January 2021

Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders

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https://api.crossref.org/works/10.1016%2FS0165-022X%2800%2900148-2

7 January 2021

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

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https://api.crossref.org/works/10.1016%2FS0165-022X%2800%2900148-2

7 January 2021

Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations

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7 January 2021

1 reference

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7 January 2021

Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course

1 reference

https://api.crossref.org/works/10.1016%2FS0165-022X%2800%2900148-2

7 January 2021

Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.

1 reference

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7 January 2021

10.1016/S0165-022X(00)00148-2

Identifiers

DOI

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4 November 2019

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