✦ LIBER ✦

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li–Fraumeni syndrome

✍ Scribed by Birch, Jillian M; Blair, Valerie; Kelsey, Anna M; Evans, D Gareth; Harris, Martin; Tricker, Karen J; Varley, Jennifer M

Book ID: 110061516
Publisher: Nature Publishing Group
Year: 1998
Tongue: English
Weight: 287 KB
Volume: 17
Category: Article
ISSN: 0950-9232
DOI: 10.1038/sj.onc.1202033

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Screening for TP53 rearrangements in fam

Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene

✍ Bougeard, Gaëlle; Brugières, Laurence; Chompret, Agnès; Gesta, Paul; Charbonnier 📂 Article 📅 2003 🏛 Nature Publishing Group 🌐 English ⚖ 195 KB

Characterization of the oligomerization

Characterization of the oligomerization defects of two p53 mutants found in families with Li–Fraumeni and Li–Fraumeni-like syndrome

✍ Davison, Timothy S; Yin, Peter; Nie, Eileen; Kay, Cyril; Arrowsmith, Cheryl H 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 306 KB

Germ-line transmission of a mutated p53

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome

✍ Srivastava, Shiv; Zou, Zhiqiang; Pirollo, Kathleen; Blattner, William; Chang, Es 📂 Article 📅 1990 🏛 Nature Publishing Group 🌐 English ⚖ 462 KB

Is there anticipation in the age at onse

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

✍ M. Trkova; M. Hladikova; P. Kasal; P. Goetz; Z. Sedlacek 📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 53 KB

A novel TP53 splicing mutation in a Li-F

A novel TP53 splicing mutation in a Li-Fraumeni syndrome family: a patient with Wilms' tumour is not a mutation carrier

✍ Varley, JM; McGown, G; Thorncroft, M; White, GRM; Tricker, KJ; Kelsey, AM; Birch 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 428 KB

GTF2I hemizygosity implicated in mental

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype-phenotype analysis of five families with deletions in the Williams syndrome region

✍ Morris, Colleen A. ;Mervis, Carolyn B. ;Hobart, Holly H. ;Gregg, Ronald G. ;Bert 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB 👁 3 views