Mendelian inheritance in man and its online version, OMIM

被引：500

作者：

McKusick, Victor A. ^{[1
]}

机构：

[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21218 USA

来源：

关键词：

D O I：

10.1086/514346

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：588 / 604

页数：17

共 81 条

[1] Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
Aitman, TJ
Dong, R
Vyse, TJ
Norsworthy, PJ
Johnson, MD
Smith, J
Mangion, J
Roberton-Lowe, C
Marshall, AJ
Petretto, E
Hodges, MD
Bhangal, G
Patel, SG
Sheehan-Rooney, K
Duda, M
Cook, PR
Evans, DJ
Domin, J
Flint, J
Boyle, JJ
Pusey, CD
Cook, HT
[J]. NATURE, 2006, 439 (7078) : 851 - 855
[2] [Anonymous], 1992, MENDELIAN INHERITANC
[3] Opinion - Mendelian disorders deserve more attention
Antonarakis, SE
Beckmann, JS
[J]. NATURE REVIEWS GENETICS, 2006, 7 (04) : 277 - 282
[4] OMIM passes the 1,000-disease-gene mark
Antonarakis, SE
McKusick, VA
[J]. NATURE GENETICS, 2000, 25 (01) : 11 - 11
[5] Antonarakis SE, 1998, HUM MUTAT, V11, P1
[6] FURTHER EVIDENCE FOR LOCATION OF THE SPHEROCYTOSIS GENE ON CHROMOSOME-8
BASS, EB
SMITH, SW
STEVENSON, RE
ROSSE, WF
[J]. ANNALS OF INTERNAL MEDICINE, 1983, 99 (02) : 192 - 193
[7] The common variants/multiple disease hypothesis of common complex genetic disorders
Becker, KG
[J]. MEDICAL HYPOTHESES, 2004, 62 (02) : 309 - 317
[8] BERGSMA D, 1969, Birth Defects Original Article Series, V5, P1
[9] BUCKLE VJ, 1984, CLIN GENET, V26, P1, DOI 10.1111/j.1399-0004.1984.tb00780.x
[10] Burchfield R., 1991, UNLOCKING ENGLISH LA