共 16 条
Genetics - The land between Mendelian and multifactorial inheritance
被引:51
作者:

Burghes, AHM
论文数: 0 引用数: 0
h-index: 0
机构:
Ohio State Univ, Dept Mol & Cellular Biol, Columbus, OH 43210 USA Ohio State Univ, Dept Mol & Cellular Biol, Columbus, OH 43210 USA

Vaessin, HEF
论文数: 0 引用数: 0
h-index: 0
机构: Ohio State Univ, Dept Mol & Cellular Biol, Columbus, OH 43210 USA

de la Chapelle, A
论文数: 0 引用数: 0
h-index: 0
机构: Ohio State Univ, Dept Mol & Cellular Biol, Columbus, OH 43210 USA
机构:
[1] Ohio State Univ, Dept Mol & Cellular Biol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Neurol, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
[4] Ohio State Univ, Neurobiotech Ctr, Columbus, OH 43210 USA
[5] Ohio State Univ, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA
来源:
关键词:
D O I:
10.1126/science.1065930
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
引用
收藏
页码:2213 / 2214
页数:2
相关论文
共 16 条
[1]
A network of interacting transcriptional regulators involved in Drosophila neural fate specification revealed by the yeast two-hybrid system
[J].
Alifragis, P
;
Poortinga, G
;
Parkhurst, SM
;
Delidakis, C
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1997, 94 (24)
:13099-13104

Alifragis, P
论文数: 0 引用数: 0
h-index: 0
机构: FDN RES & TECHNOL HELLAS, INST MOL BIOL & BIOTECHNOL, GR-71110 IRAKLION, GREECE

Poortinga, G
论文数: 0 引用数: 0
h-index: 0
机构: FDN RES & TECHNOL HELLAS, INST MOL BIOL & BIOTECHNOL, GR-71110 IRAKLION, GREECE

Parkhurst, SM
论文数: 0 引用数: 0
h-index: 0
机构: FDN RES & TECHNOL HELLAS, INST MOL BIOL & BIOTECHNOL, GR-71110 IRAKLION, GREECE

Delidakis, C
论文数: 0 引用数: 0
h-index: 0
机构: FDN RES & TECHNOL HELLAS, INST MOL BIOL & BIOTECHNOL, GR-71110 IRAKLION, GREECE
[2]
GENETIC-ANALYSIS OF A DROSOPHILA NEURAL CELL-ADHESION MOLECULE - INTERACTION OF FASCICLIN-I AND ABELSON TYROSINE KINASE MUTATIONS
[J].
ELKINS, T
;
ZINN, K
;
MCALLISTER, L
;
HOFFMANN, FM
;
GOODMAN, CS
.
CELL,
1990, 60 (04)
:565-575

ELKINS, T
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF BERKELEY,HOWARD HUGHES MED INST,BERKELEY,CA 94720

ZINN, K
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF BERKELEY,HOWARD HUGHES MED INST,BERKELEY,CA 94720

MCALLISTER, L
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF BERKELEY,HOWARD HUGHES MED INST,BERKELEY,CA 94720

HOFFMANN, FM
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF BERKELEY,HOWARD HUGHES MED INST,BERKELEY,CA 94720

GOODMAN, CS
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF BERKELEY,HOWARD HUGHES MED INST,BERKELEY,CA 94720
[3]
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
[J].
Hugot, JP
;
Chamaillard, M
;
Zouali, H
;
Lesage, S
;
Cézard, JP
;
Belaiche, J
;
Almer, S
;
Tysk, C
;
O'Morain, CA
;
Gassull, M
;
Binder, V
;
Finkel, Y
;
Cortot, A
;
Modigliani, R
;
Laurent-Puig, P
;
Gower-Rousseau, C
;
Macry, J
;
Colombel, JF
;
Sahbatou, M
;
Thomas, G
.
NATURE,
2001, 411 (6837)
:599-603

Hugot, JP
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Chamaillard, M
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Zouali, H
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Lesage, S
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Cézard, JP
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Belaiche, J
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Almer, S
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Tysk, C
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

O'Morain, CA
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Gassull, M
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Binder, V
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Finkel, Y
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Cortot, A
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Modigliani, R
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Laurent-Puig, P
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Gower-Rousseau, C
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Macry, J
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Colombel, JF
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Sahbatou, M
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France

Thomas, G
论文数: 0 引用数: 0
h-index: 0
机构: Fdn Jean Dausset CEPH, F-75010 Paris, France
[4]
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder
[J].
Katsanis, N
;
Ansley, SJ
;
Badano, JL
;
Eichers, ER
;
Lewis, RA
;
Hoskins, BE
;
Scambler, PJ
;
Davidson, WS
;
Beales, PL
;
Lupski, JR
.
SCIENCE,
2001, 293 (5538)
:2256-2259

Katsanis, N
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Ansley, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Badano, JL
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Eichers, ER
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

论文数: 引用数:
h-index:
机构:

Hoskins, BE
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Scambler, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Davidson, WS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Beales, PL
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Lupski, JR
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[5]
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome
[J].
Katsanis, N
;
Beales, PL
;
Woods, MO
;
Lewis, RA
;
Green, JS
;
Parfrey, PS
;
Ansley, SJ
;
Davidson, WS
;
Lupski, JR
.
NATURE GENETICS,
2000, 26 (01)
:67-70

Katsanis, N
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Beales, PL
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Woods, MO
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

论文数: 引用数:
h-index:
机构:

Green, JS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Parfrey, PS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Ansley, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Davidson, WS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA

Lupski, JR
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Human Mol Genet, Houston, TX 77030 USA
[6]
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number
[J].
McAndrew, PE
;
Parsons, DW
;
Simard, LR
;
Rochette, C
;
Ray, PN
;
Mendell, JR
;
Prior, TW
;
Burghes, AHM
.
AMERICAN JOURNAL OF HUMAN GENETICS,
1997, 60 (06)
:1411-1422

McAndrew, PE
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Parsons, DW
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Simard, LR
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Rochette, C
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Ray, PN
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Mendell, JR
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Prior, TW
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210

Burghes, AHM
论文数: 0 引用数: 0
h-index: 0
机构: OHIO STATE UNIV,DEPT PATHOL,COLUMBUS,OH 43210
[7]
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
[J].
Mykytyn, K
;
Braun, T
;
Carmi, R
;
Haider, NB
;
Searby, CC
;
Shastri, M
;
Beck, G
;
Wright, AF
;
Iannaccone, A
;
Elbedour, K
;
Riise, R
;
Baldi, A
;
Raas-Rothschild, A
;
Gorman, SW
;
Duhl, DM
;
Jacobson, SG
;
Casavant, T
;
Stone, EM
;
Sheffield, VC
.
NATURE GENETICS,
2001, 28 (02)
:188-191

Mykytyn, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Braun, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Carmi, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Haider, NB
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Searby, CC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Shastri, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Beck, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Wright, AF
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

论文数: 引用数:
h-index:
机构:

Elbedour, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Riise, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Baldi, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Raas-Rothschild, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Gorman, SW
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Duhl, DM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Jacobson, SG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Casavant, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Stone, EM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA

Sheffield, VC
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA Univ Iowa, Dept Pediat, Div Med Genet, Iowa City, IA 52242 USA
[8]
Modifier genes in mice and humans
[J].
Nadeau, JH
.
NATURE REVIEWS GENETICS,
2001, 2 (03)
:165-174

Nadeau, JH
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
[9]
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
[J].
Nishimura, DY
;
Searby, CC
;
Carmi, R
;
Elbedour, K
;
Van Maldergem, L
;
Fulton, AB
;
Lam, BL
;
Powell, BR
;
Swiderski, RE
;
Bugge, KE
;
Haider, NB
;
Kwitek-Black, AE
;
Ying, LH
;
Duhl, DM
;
Gorman, SW
;
Heon, E
;
Iannaccone, A
;
Bonneau, D
;
Biesecker, LG
;
Jacobson, SG
;
Stone, EM
;
Sheffield, VC
.
HUMAN MOLECULAR GENETICS,
2001, 10 (08)
:865-874

Nishimura, DY
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Searby, CC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Carmi, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Elbedour, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Van Maldergem, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Fulton, AB
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Lam, BL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Powell, BR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Swiderski, RE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Bugge, KE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Haider, NB
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Kwitek-Black, AE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Ying, LH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Duhl, DM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Gorman, SW
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Heon, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Iannaccone, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Bonneau, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Biesecker, LG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Jacobson, SG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Stone, EM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA

Sheffield, VC
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[10]
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
[J].
Ogura, Y
;
Bonen, DK
;
Inohara, N
;
Nicolae, DL
;
Chen, FF
;
Ramos, R
;
Britton, H
;
Moran, T
;
Karaliuskas, R
;
Duerr, RH
;
Achkar, JP
;
Brant, SR
;
Bayless, TM
;
Kirschner, BS
;
Hanauer, SB
;
Nuñez, G
;
Cho, JH
.
NATURE,
2001, 411 (6837)
:603-606

Ogura, Y
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Bonen, DK
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Inohara, N
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Nicolae, DL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Chen, FF
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Ramos, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Britton, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Moran, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Karaliuskas, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Duerr, RH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Achkar, JP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Brant, SR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Bayless, TM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Kirschner, BS
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Hanauer, SB
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Nuñez, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA

Cho, JH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA