Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p.
作者信息
Vitale E, Brancolini V, De Rienzo A, Bird L, Allada V, Sklansky M, Chae C U, Ferrero G B, Weber J, Devoto M, Casey B
出版信息
J Med Genet. 2001 Mar;38(3):182-5. doi: 10.1136/jmg.38.3.182.
Abstract
摘要
相似文献
1
Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p.
J Med Genet. 2001 Mar;38(3):182-5. doi: 10.1136/jmg.38.3.182.
2
Two rights make a wrong: human left-right malformations.
Hum Mol Genet. 1998;7(10):1565-71. doi: 10.1093/hmg/7.10.1565.
3
Congenital heart disease and the specification of left-right asymmetry.
Am J Physiol Heart Circ Physiol. 2012 May 15;302(10):H2102-11. doi: 10.1152/ajpheart.01118.2011. Epub 2012 Mar 9.
4
Clinical analysis of families with heart, midline, and laterality defects.
Am J Med Genet. 2001 Jul 15;101(4):388-92. doi: 10.1002/ajmg.1221.
5
Disorders of left-right asymmetry: heterotaxy and situs inversus.
Am J Med Genet C Semin Med Genet. 2009 Nov 15;151C(4):307-17. doi: 10.1002/ajmg.c.30228.
6
Left-right patterning in congenital heart disease beyond heterotaxy.
Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):90-96. doi: 10.1002/ajmg.c.31768. Epub 2020 Jan 30.
7
X-linked situs abnormalities result from mutations in ZIC3.
Nat Genet. 1997 Nov;17(3):305-8. doi: 10.1038/ng1197-305.
8
Cardiopulmonary malformations in the inv/inv mouse.
Anat Rec. 2001 May 1;263(1):62-71. doi: 10.1002/ar.1077.
9
Familial situs inversus and congenital heart defects.
Am J Med Genet. 1988 Nov;31(3):689-90. doi: 10.1002/ajmg.1320310325.
10
X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.
Am J Med Genet. 1987 Sep;28(1):111-6. doi: 10.1002/ajmg.1320280116.
引用本文的文献
1
The determination factors of left-right asymmetry disorders- a short review.
Clujul Med. 2017;90(2):139-146. doi: 10.15386/cjmed-701. Epub 2017 Apr 25.
2
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Eur J Hum Genet. 2016 Dec;24(12):1783-1791. doi: 10.1038/ejhg.2016.91. Epub 2016 Jul 13.
3
A Rare Triad of Giant Occipital Encephalocele with Lipomyelomeningocele, Tetralogy of Fallot, and Situs Inversus.
J Radiol Case Rep. 2016 Mar 31;10(3):36-46. doi: 10.3941/jrcr.v10i3.2718. eCollection 2016 Mar.
4
Genetic and functional analyses of ZIC3 variants in congenital heart disease.
Hum Mutat. 2014 Jan;35(1):66-75. doi: 10.1002/humu.22457.
5
NPHP4 variants are associated with pleiotropic heart malformations.
Circ Res. 2012 Jun 8;110(12):1564-74. doi: 10.1161/CIRCRESAHA.112.269795. Epub 2012 May 1.
6
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
Hum Genet. 2008 Jan;122(6):595-603. doi: 10.1007/s00439-007-0436-x. Epub 2007 Oct 16.
7
Split cord malformation and situs inversus totalis: case report and review of the literature.
Childs Nerv Syst. 2005 Feb;21(2):161-4. doi: 10.1007/s00381-003-0895-x. Epub 2004 Jan 23.
8
Split cord malformation and situs inversus totalis: case report and review of the literature.
Childs Nerv Syst. 2004 Feb;20(2):131-4. doi: 10.1007/s00381-003-0857-3. Epub 2003 Nov 26.
Zotero 插件