共 153 条
[1]
Genome-wide analyses of human perisylvian cerebral cortical patterning
[J].
Abrahams, B. S.
;
Tentler, D.
;
Perederiy, J. V.
;
Oldham, M. C.
;
Coppola, G.
;
Geschwind, D. H.
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
2007, 104 (45)
:17849-17854

Abrahams, B. S.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA

Tentler, D.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA

Perederiy, J. V.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA

Oldham, M. C.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA

Coppola, G.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA

Geschwind, D. H.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Behavior, Dept Neurol,Program Neurogenet & Neurobehavioral, Los Angeles, CA 90095 USA
[2]
ABRAHAMS BS, 2005, ENCY GENETICS GENOMI, P1
[3]
Gene prioritization through genomic data fusion
[J].
Aerts, S
;
Lambrechts, D
;
Maity, S
;
Van Loo, P
;
Coessens, B
;
De Smet, F
;
Tranchevent, LC
;
De Moor, B
;
Marynen, P
;
Hassan, B
;
Carmeliet, P
;
Moreau, Y
.
NATURE BIOTECHNOLOGY,
2006, 24 (05)
:537-544

Aerts, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Lambrechts, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Maity, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Van Loo, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Coessens, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

De Smet, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Tranchevent, LC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

De Moor, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Marynen, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Hassan, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Carmeliet, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium

Moreau, Y
论文数: 0 引用数: 0
h-index: 0
机构: Univ Leuven VIB, Neurogenet Lab, Dept Human Genet, B-3000 Louvain, Belgium
[4]
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
[J].
Alarcón, M
;
Yonan, AL
;
Gilliam, TC
;
Cantor, RM
;
Geschwind, DH
.
MOLECULAR PSYCHIATRY,
2005, 10 (08)
:747-757

Alarcón, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Ctr Neurobehav Genet, Dept Neurol, Los Angeles, CA 90095 USA

Yonan, AL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Ctr Neurobehav Genet, Dept Neurol, Los Angeles, CA 90095 USA

论文数: 引用数:
h-index:
机构:

Cantor, RM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Ctr Neurobehav Genet, Dept Neurol, Los Angeles, CA 90095 USA

Geschwind, DH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Ctr Neurobehav Genet, Dept Neurol, Los Angeles, CA 90095 USA
[5]
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
[J].
Alarcón, M
;
Cantor, RM
;
Liu, JJ
;
Gilliam, TC
;
Geschwind, DH
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2002, 70 (01)
:60-71

Alarcón, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Dept Neurol, Reed Neurol Res Ctr, Sch Med, Los Angeles, CA 90095 USA

Cantor, RM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Dept Neurol, Reed Neurol Res Ctr, Sch Med, Los Angeles, CA 90095 USA

Liu, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Dept Neurol, Reed Neurol Res Ctr, Sch Med, Los Angeles, CA 90095 USA

Gilliam, TC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Dept Neurol, Reed Neurol Res Ctr, Sch Med, Los Angeles, CA 90095 USA

Geschwind, DH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Dept Neurol, Reed Neurol Res Ctr, Sch Med, Los Angeles, CA 90095 USA
[6]
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
[J].
Alarcon, Maricela
;
Abrahams, Brett S.
;
Stone, Jennifer L.
;
Duvall, Jacqueline A.
;
Perederiy, Julia V.
;
Bomar, Jamee M.
;
Sebat, Jonathan
;
Wigler, Michael
;
Martin, Christa L.
;
Ledbetter, David H.
;
Nelson, Stanley E.
;
Cantor, Rita M.
;
Geschwind, Daniel H.
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2008, 82 (01)
:150-159

Alarcon, Maricela
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Abrahams, Brett S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Stone, Jennifer L.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Duvall, Jacqueline A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Perederiy, Julia V.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Bomar, Jamee M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Sebat, Jonathan
论文数: 0 引用数: 0
h-index: 0
机构:
Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Wigler, Michael
论文数: 0 引用数: 0
h-index: 0
机构:
Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Martin, Christa L.
论文数: 0 引用数: 0
h-index: 0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Ledbetter, David H.
论文数: 0 引用数: 0
h-index: 0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Nelson, Stanley E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Cantor, Rita M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA

Geschwind, Daniel H.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, UCLA Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, UCLA Ctr Autism Res & Treatment, Semel Inst Neurosci, Los Angeles, CA 90095 USA
[7]
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
[J].
Amir, RE
;
Van den Veyver, IB
;
Wan, M
;
Tran, CQ
;
Francke, U
;
Zoghbi, HY
.
NATURE GENETICS,
1999, 23 (02)
:185-188

Amir, RE
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Van den Veyver, IB
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Wan, M
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Tran, CQ
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Francke, U
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Zoghbi, HY
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[8]
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
[J].
Arking, Dan E.
;
Cutler, David J.
;
Brune, Camille W.
;
Teslovich, Tanya M.
;
West, Kristen
;
Ikeda, Morna
;
Rea, Alexis
;
Guy, Moltu
;
Lin, Shin
;
Cook, Edwin H., Jr.
;
Chakravarti, Aravinda
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2008, 82 (01)
:160-164

Arking, Dan E.
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Cutler, David J.
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Brune, Camille W.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Illinois, Dept Psychiat, Inst Juvenile Res, Chicago, IL 60612 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Teslovich, Tanya M.
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

West, Kristen
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Ikeda, Morna
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Rea, Alexis
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Guy, Moltu
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Lin, Shin
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Cook, Edwin H., Jr.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Illinois, Dept Psychiat, Inst Juvenile Res, Chicago, IL 60612 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA

Chakravarti, Aravinda
论文数: 0 引用数: 0
h-index: 0
机构:
Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[9]
Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans
[J].
Arya, R
;
Duggirala, R
;
Almasy, L
;
Rainwater, DL
;
Mahaney, MC
;
Cole, S
;
Dyer, TD
;
Williams, K
;
Leach, RJ
;
Hixson, JE
;
MacCluer, JW
;
O'Connell, P
;
Stern, MP
;
Blangero, J
.
NATURE GENETICS,
2002, 30 (01)
:102-105

Arya, R
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Duggirala, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Almasy, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Rainwater, DL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Mahaney, MC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Cole, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Dyer, TD
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Williams, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Leach, RJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Hixson, JE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

MacCluer, JW
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

O'Connell, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Stern, MP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA

Blangero, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA
[10]
A genomewide screen for autism-spectrum disorders:: Evidence for a major susceptibility locus on chromosome 3q25-27
[J].
Auranen, M
;
Vanhala, R
;
Varilo, T
;
Ayers, K
;
Kempas, E
;
Ylisaukko-oja, T
;
Sinsheimer, JS
;
Peltonen, L
;
Järvelä, I
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2002, 71 (04)
:777-790

Auranen, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Vanhala, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Varilo, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Ayers, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Kempas, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Ylisaukko-oja, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Sinsheimer, JS
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Peltonen, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland

Järvelä, I
论文数: 0 引用数: 0
h-index: 0
机构: Univ Helsinki, Dept Med Genet, Biomedicum, Helsinki 00290, Finland
