文献
J-GLOBAL ID:201202283912294403
整理番号:12A0934013
Cantu症候群はABCC9の突然変異に起因する
Cantu Syndrome Is Caused by Mutations in ABCC9
著者 (23件):
VAN BON Bregje W.M.
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
GILISSEN Christian
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
GRANGE Dorothy K.
(Dep. of Pediatrics, Div. of Genetics and Genomic Medicine, Washington Univ. School of Medicine, St. Louis, MO 63110, USA)
,
HENNEKAM Raoul C.M.
(Dep. of Paediatrics and Translational Genetics, Academic Medical Center, Univ. of Amsterdam, 1105AZ Amsterdam, NLD)
,
KAYSERILI Huelya
(Medical Genetics Dep., Istanbul Medical Fac., Istanbul Univ., Istanbul 34093, TUR)
,
ENGELS Hartmut
(Inst. of Human Genetics, Univ. of Bonn, 53127 Bonn, DEU)
,
REUTTER Heiko
(Inst. of Human Genetics, Univ. of Bonn, 53127 Bonn, DEU)
,
REUTTER Heiko
(Dep. of Neonatology, Children’s Hospital, Univ. of Bonn, 53127 Bonn, DEU)
,
OSTERGAARD John R.
(Centre for Rare Diseases, Dep. of Pediatrics, Aarhus Univ. Hospital Skejby, 8200 Aarhus N, DNK)
,
MORAVA Eva
(Dep. of Pediatrics and Inst. for Genetic and Metabolic Disease, Radboud Univ. Nijmegen Medical Centre, Radboud Univ. ...)
,
TSIAKAS Konstantinos
(Dep. of Pediatrics, Univ. Medical Center Eppendorf, 20246 Hamburg, DEU)
,
ISIDOR Bertrand
(Clinical Genetics Unit, Univ. Hospital Nantes, Nantes 44093, FRA)
,
LE MERRER Martine
(Dep. de Genetique, Univ. Paris Descartes, Hopital Necker-Enfants Malades, Paris 75015, FRA)
,
ESER Metin
(Medical Genetics Dep., Istanbul Medical Fac., Istanbul Univ., Istanbul 34093, TUR)
,
WIESKAMP Nienke
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
DE VRIES Petra
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
STEEHOUWER Marloes
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
VELTMAN Joris A.
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
ROBERTSON Stephen P.
(Dep. of Paediatrics and Child Health, Dunedin School of Medicine, Univ. of Otago, Dunedin 9054, NZL)
,
BRUNNER Han G.
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
DE VRIES Bert B.A.
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
HOISCHEN Alexander
(Dep. of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Inst. for Genetic and Metabolic Disorders ...)
,
HOISCHEN Alexander
(Center for Medical Genetics and Molecular Medicine, Haukeland Univ. Hospital, 5021 Bergen, NOR)
資料名:
American Journal of Human Genetics
(American Journal of Human Genetics)
巻:
90
号:
6
ページ:
1094-1101
発行年:
2012年06月08日
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)