Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) -: art. no. e32

被引：47

作者：

Villablanca, A ^{[1
]}

Calender, A

Forsberg, L

Höög, A

Cheng, JD

Petillo, D

Bauters, C

Kahnoski, K

Ebeling, T

Salmela, P

Richardson, AL

Delbridge, L

Meyrier, A

Proye, C

Carpten, JD

Teh, BT

Robinson, BG

Larsson, C

机构：

[1] Karolinska Hosp, Dept Mol Med, S-10401 Stockholm, Sweden

[2] Karolinska Hosp, Dept Oncol Pathol, S-10401 Stockholm, Sweden

[3] Canc Genet Lab, CNRS, UMR, Lyon, France

[4] Van Andel Res Inst, Grand Rapids, MI USA

[5] CHRU Lille, Serv Endocrinol, Lille, France

[6] Oulu Univ Hosp, Dept Internal Med, Oulu, Finland

[7] Royal N Shore Hosp, Kolling Inst Med Res, Canc Genet Unit, Sydney, NSW, Australia

[8] Univ Sydney, Dept Mol Med, Sydney, NSW 2006, Australia

[9] Hop Broussais, Serv Nephrol, F-75674 Paris, France

[10] CHRU Lille, Serv Chirurg Endocrine, Lille, France

[11] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 03期

关键词：

D O I：

10.1136/jmg.2003.012369

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：7

共 33 条

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