文献
J-GLOBAL ID:200902202277631591
整理番号:07A0962200
Marfan症候群又は関連表現型とFBN1突然変異初回被患者1013名の臨床転帰に及ぼす突然変異型と位置の効果:国際的研究
Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study
著者 (40件):
FAIVRE L.
(Centre Hospitalier Universitaire (CHU))
,
FAIVRE L.
(Centre d’Investigation Clinique-Epidemiologie Clinique/Essais Cliniques)
,
COLLOD-BEROUD G.
(INSERM U827)
,
COLLOD-BEROUD G.
(Univ. Montpellier I)
,
LOEYS B. L.
(Ghent Univ. Hospital, Ghent, BEL)
,
LOEYS B. L.
(Johns Hopkins Univ. School of Medicine, Baltimore)
,
CHILD A.
(St. George’s Hospital, London)
,
BINQUET C.
(Centre d’Investigation Clinique-Epidemiologie Clinique/Essais Cliniques)
,
BINQUET C.
(INSERM CIE1, Dijon, FRA)
,
GAUTIER E.
(Centre d’Investigation Clinique-Epidemiologie Clinique/Essais Cliniques)
,
GAUTIER E.
(INSERM CIE1, Dijon, FRA)
,
CALLEWAERT B.
(Ghent Univ. Hospital, Ghent, BEL)
,
ARBUSTINI E.
(Foundation IRCCS Policlinico San Matteo, Pavia, ITA)
,
MAYER K.
(Center for Human Genetics and Lab. Medicine, Martinsried, DEU)
,
ARSLAN-KIRCHNER M.
(Hannover Medical School, Hannover)
,
KIOTSEKOGLOU A.
(St. George’s Hospital, London)
,
COMEGLIO P.
(St. George’s Hospital, London)
,
MARZILIANO N.
(Foundation IRCCS Policlinico San Matteo, Pavia, ITA)
,
DIETZ H. C.
(Johns Hopkins Univ. School of Medicine, Baltimore)
,
HALLIDAY D.
(Univ. Oxford, Oxford, GBR)
,
BEROUD C.
(INSERM U827)
,
BEROUD C.
(Univ. Montpellier I)
,
BEROUD C.
(CHU Montpellier, Montpellier, FRA)
,
BONITHON-KOPP C.
(Centre d’Investigation Clinique-Epidemiologie Clinique/Essais Cliniques)
,
BONITHON-KOPP C.
(INSERM CIE1, Dijon, FRA)
,
CLAUSTRES M.
(INSERM U827)
,
CLAUSTRES M.
(Univ. Montpellier I)
,
CLAUSTRES M.
(CHU Montpellier, Montpellier, FRA)
,
MUTI C.
(Univ. Versailles-Saint Quentin en Yvelines, Boulogne, FRA)
,
PLAUCHU H.
(Hotel Dieu, Lyon)
,
ROBINSON P. N.
(Universitaetsmedizin Charite, Berlin)
,
ADES L. C.
(Children’s Hospital at Westmead, Sydney, AUS)
,
BIGGIN A.
(Children’s Hospital at Westmead, Sydney, AUS)
,
BENETTS B.
(Children’s Hospital at Westmead, Sydney, AUS)
,
BRETT M.
(Children’s Hospital at Westmead, Sydney, AUS)
,
HOLMAN K. J.
(Children’s Hospital at Westmead, Sydney, AUS)
,
DE BACKER J.
(Ghent Univ. Hospital, Ghent, BEL)
,
COUCKE P.
(Ghent Univ. Hospital, Ghent, BEL)
,
FRANCKE U.
(Stanford Univ. Medical Center, Stanford)
,
DE PAEPE A.
(Ghent Univ. Hospital, Ghent, BEL)
資料名:
American Journal of Human Genetics
(American Journal of Human Genetics)
巻:
81
号:
3
ページ:
454-466
発行年:
2007年09月
JST資料番号:
B0360B
ISSN:
0002-9297
資料種別:
逐次刊行物 (A)
発行国:
オランダ (NLD)
言語:
英語 (EN)