Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.

Teh, BT (author)

Farnebo, F (author)

Phelan, C (author)

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Cardinal, J (author)

Cameron, D (author)

Edwards, M (author)

Epsein, M (author)

Hurley, D (author)

Sheppherd, JJ (author)

Larsson, C (author)

Kytola, S (author)

Tranebjaerg, L (author)

Jorde, R (author)

Leisti, J (author)

Samela, P (author)

Khodaei, S (author)

Parente, F (author)

Nordenskjold, M (author)

Weber, G (author)

Bergman, L (author)

Hayward, N (author)

Grimmond, S (author)

Silins, G (author)

Walters, M (author)

Stewart, C (author)

Skogseid, B (author)

Uppsala universitet,Institutionen för medicinska vetenskaper

Oberg, K (author)

Uppsala universitet,Institutionen för medicinska vetenskaper

Menon, J (author)

Khir, A (author)

Tan, TT (author)

Chan, SP (author)

Zaini, A (author)

Khalid, BAK (author)

Sandelin, K (author)

Thompson, N (author)

Brandi, M-L (author)

Waugh, M (author)

Stock, J (author)

Beckers, A (author)

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 (creator_code:org_t)

1998

1998

English.

In: J Clin Endocrinol Metab. ; 83, s. 2621-

Related links:

https://urn.kb.se/re...

• Journal article (peer-reviewed)