Literature DB >> 1671132

Presymptomatic screening for MEN-2A.

P J Morrison, N C Nevin, A E Hughes, D R Hadden, C F Russell.   

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Year:  1991        PMID： 1671132     DOI： 10.1016/0140-6736(91)90908-8

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Epidemiology, clinical features, and genetics of multiple endocrine neoplasia type 2B in a complete population.

Authors:  Anna Znaczko; Deirdre E Donnelly; Patrick J Morrison
Journal:  Oncologist       Date:  2014-10-29

2.  The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype with incomplete penetrance: implications for screening and management of carrier status.

Authors:  Tabib Dabir; Steven J Hunter; Colin F J Russell; Damien McCall; Patrick J Morrison
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

Review 3.  Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).

Authors:  P J Morrison; N C Nevin
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318
  3 in total

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