Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.
about
Molecular genetics of hereditary renal cancer: new genes and diagnostic and therapeutic opportunities.Molecular diagnosis of primary hyperparathyroidism in familial cancer syndromes.CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort
P2860
Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@ast
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@en
type
label
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@ast
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@en
prefLabel
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@ast
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@en
P2093
P2860
P1476
Rapid mutation screening for H ...... c primary hyperparathyroidism.
@en
P2093
Anne-Louise Richardson
Bruce G Robinson
Deborah J Marsh
John W Cardinal
Oliver Gimm
Viive M Howell
P2860
P304
P356
10.2353/JMOLDX.2006.060015
P577
2006-11-01T00:00:00Z