Literature DB >> 8621242

Evidence of a hereditary p53 syndrome in cancer-prone families.

Q Wang, C Lasset, H Sobol, M Ozturk.   

Abstract

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Mesh：

Year:  1996        PMID： 8621242

Source DB:  PubMed          Journal:  Int J Cancer        ISSN： 0020-7136            Impact factor:   7.396


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  3 in total

1.  Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours.

Authors:  Z Sedlacek; R Kodet; V Kriz; E Seemanova; P Vodvarka; P Wilgenbus; J Mares; A Poustka; P Goetz
Journal:  Br J Cancer       Date:  1998-04       Impact factor: 7.640

2.  No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours.

Authors:  S Jefferies; S M Edwards; R A Hamoudi; R A'Hern; W Foulkes; D Goldgar; R Eeles
Journal:  Br J Cancer       Date:  2001-11-02       Impact factor: 7.640

3.  Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families.

Authors:  M Zelada-Hedman; A L Børresen-Dale; A Claro; J Chen; L Skoog; A Lindblom
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640
  3 in total

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