Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL

P Pajukanta; JS Bodnar; R Sallinen; M Chu; T Airaksinen; QN Xiao; LW Castellani; SS Sheth; M Wessman; A Palotie; JS Sinsheimer; P Demant; AJ Lusis; L Peltonen

Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL

P Pajukanta, JS Bodnar, R Sallinen, M Chu, T Airaksinen, QN Xiao, LW Castellani, SS Sheth, M Wessman, A Palotie, JS Sinsheimer, P Demant, AJ Lusis, L Peltonen

Suomen molekyylilääketieteen instituutti

Tutkimustuotos: Artikkelijulkaisu › Artikkeli › Tieteellinen › vertaisarvioitu

Alkuperäiskieli	englanti
Lehti	Mammalian Genome
Vuosikerta	12
Numero	3
Sivut	238-245
Sivumäärä	8
ISSN	0938-8990
Tila	Julkaistu - maalisk. 2001
OKM-julkaisutyyppi	A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Siteeraa tätä

@article{65c2e4835e0d4701b22e3af8c4578d51,

title = "Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL",

keywords = "FAMILIAL COMBINED HYPERLIPIDEMIA, CORONARY-ARTERY DISEASE, AIV GENE-CLUSTER, CHROMOSOME 1Q21-Q23, FINNISH FAMILIES, COMPLEX TRAITS, HEART-DISEASE, LINKAGE, HYBRIDIZATION, CHOLESTEROL",

author = "P Pajukanta and JS Bodnar and R Sallinen and M Chu and T Airaksinen and QN Xiao and LW Castellani and SS Sheth and M Wessman and A Palotie and JS Sinsheimer and P Demant and AJ Lusis and L Peltonen",

year = "2001",

month = mar,

language = "English",

volume = "12",

pages = "238--245",

journal = "Mammalian Genome",

issn = "0938-8990",

publisher = "Springer",

number = "3",

}

TY - JOUR

T1 - Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL

AU - Pajukanta, P

AU - Bodnar, JS

AU - Sallinen, R

AU - Chu, M

AU - Airaksinen, T

AU - Xiao, QN

AU - Castellani, LW

AU - Sheth, SS

AU - Wessman, M

AU - Palotie, A

AU - Sinsheimer, JS

AU - Demant, P

AU - Lusis, AJ

AU - Peltonen, L

PY - 2001/3

Y1 - 2001/3

KW - FAMILIAL COMBINED HYPERLIPIDEMIA

KW - CORONARY-ARTERY DISEASE

KW - AIV GENE-CLUSTER

KW - CHROMOSOME 1Q21-Q23

KW - FINNISH FAMILIES

KW - COMPLEX TRAITS

KW - HEART-DISEASE

KW - LINKAGE

KW - HYBRIDIZATION

KW - CHOLESTEROL

M3 - Article

SN - 0938-8990

VL - 12

SP - 238

EP - 245

JO - Mammalian Genome

JF - Mammalian Genome

IS - 3

ER -