Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations

被引：17

作者：

Dahia, PM

Gimm, O

Chi, HB

Marsh, DJ

Reynolds, PR

Eng, C

机构：

[1] Ohio State Univ, Ctr Comprehens Canc, Clin Canc Genet Program, Columbus, OH 43210 USA

[2] Ohio State Univ, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA

[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

[4] Univ Rochester, Sch Med, Dept Orthopaed, Rochester, NY USA

[5] Univ Cambridge, CRC, Human Canc Genet Res Grp, Cambridge, England

来源：

JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷 / 09期

关键词：

D O I：

10.1136/jmg.37.9.715

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：715 / 717

页数：3

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