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MEN1 gene mutations are a rare event in patients with sporadic neuroendocrine tumors

✍ Scribed by C Asteria; M Anagni; L Fugazzola; G Faglia; P Vezzadini; P Beck-Peccoz


Book ID
117644233
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
121 KB
Volume
13
Category
Article
ISSN
0953-6205

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Germline LEMD3 mutations are rare in spo
✍ Jan Hellemans; Philippe Debeer; Michael Wright; Andreas Janecke; Klaus W. Kjaer; πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 173 KB πŸ‘ 1 views

To further explore the allelic heterogeneity within the group of LEMD3-related disorders, we have screened a larger series of patients including 5 probands with osteopoikilosis or Buschke-Ollendorff syndrome (BOS), 2 families with the co-occurrence of melorheostosis and BOS, and 12 unrelated patient