Genotype–phenotype correlations in Peutz-Jeghers syndrome

Background and aims: Peutz-Jeghers syndrome (PJS) is a dominantly inherited disorder often caused by mutations in STK11. Time to onset of symptoms was characterised for a large collection of individuals with PJS who had been tested for STK11 mutations and genotype–phenotype correlations were evaluat...

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Main Authors:	Amos, C, Keitheri-Cheteri, M, Sabripour, M, Wei, C, McGarrity, T, Seldin, M, Nations, L, Lynch, P, Fidder, H, Friedman, E, Frazier, M
Format:	Artigo
Language:	Inglês
Published:	BMJ Group 2004
Subjects:	Original Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1735760/ https://ncbi.nlm.nih.gov/pubmed/15121768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2003.010900
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Genotype–phenotype correlations in Peutz-Jeghers syndrome

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