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Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal.

作者信息

Gennarelli M, Novelli G, Digilio M C, Giannotti A, Marino B, Dallapiccola B

出版信息

Hum Genet. 1994 Dec;94(6):708-10. doi: 10.1007/BF00206969.

DOI:10.1007/BF00206969
PMID:7989049
Abstract
摘要

相似文献

1
Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal.
Hum Genet. 1994 Dec;94(6):708-10. doi: 10.1007/BF00206969.
2
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21.
Hum Genet. 1994 Feb;93(2):103-8. doi: 10.1007/BF00210591.
3
Down's syndrome affects results of surgical correction of complete atrioventricular canal.唐氏综合征会影响完全性房室通道手术矫正的效果。
Pediatr Cardiol. 1992 Apr;13(2):80-4. doi: 10.1007/BF00798209.
4
Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse.唐氏综合征样心脏发育缺陷在转染色体 Tc1 小鼠胚胎中。
Cardiovasc Res. 2010 Nov 1;88(2):287-95. doi: 10.1093/cvr/cvq193. Epub 2010 Jun 16.
5
Looking down the atrioventricular canal.观察房室管。
Cardiovasc Res. 2010 Nov 1;88(2):205-6. doi: 10.1093/cvr/cvq302. Epub 2010 Sep 20.
6
[Hydrops and common atrioventricular canal in a fetus of karyotype 47(XY)+21. Ultrasonic diagnosis at twenty weeks].[核型为47(XY)+21的胎儿中的水肿和共同房室通道。孕20周时的超声诊断]
Minerva Ginecol. 1990 Sep;42(9):365-7.
7
Down's syndrome, complete atrioventricular canal, and pulmonary vascular obstructive disease.唐氏综合征、完全性房室通道和肺血管阻塞性疾病。
J Thorac Cardiovasc Surg. 1990 Jul;100(1):115-21.
8
[Identification of families with increased risk of Down's syndrome caused by translocation of chromosome 9].[由9号染色体易位导致唐氏综合征风险增加的家族的鉴定]
Pediatr Pol. 1989 Apr;64(4):209-15.
9
Prevalence of left-sided obstructive lesions in patients with atrioventricular canal without Down's syndrome.
J Thorac Cardiovasc Surg. 1986 Mar;91(3):467-9.
10
A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.一个大型的、具有主导性的房室间隔缺损（AVSD）家系：排除21号染色体上的唐氏综合征关键区域。
Am J Hum Genet. 1993 Dec;53(6):1262-8.

引用本文的文献

1
Genetics of atrioventricular canal defects.房室管缺陷的遗传学。
Ital J Pediatr. 2020 May 13;46(1):61. doi: 10.1186/s13052-020-00825-4.
2
Is a shorter atrioventricular septal length an intermediate phenotype in the spectrum of nonsyndromic atrioventricular septal defects?房室间隔较短是否为非综合征性房室间隔缺损谱中的中间表型？
J Am Soc Echocardiogr. 2012 Jul;25(7):782-9. doi: 10.1016/j.echo.2012.03.011. Epub 2012 Apr 25.
3
Familial recurrence of congenital heart disease: an overview and review of the literature.先天性心脏病的家族复发：文献综述与概述

本文引用的文献

1
A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.一个大型的、具有主导性的房室间隔缺损（AVSD）家系：排除21号染色体上的唐氏综合征关键区域。
Am J Hum Genet. 1993 Dec;53(6):1262-8.
2
Risk of congenital heart defects in relatives of patients with atrioventricular canal.
Am J Dis Child. 1993 Dec;147(12):1295-7. doi: 10.1001/archpedi.1993.02160360037013.
3
Atrioventricular canal and 8p- syndrome.
Am J Med Genet. 1993 Sep 1;47(3):437-8. doi: 10.1002/ajmg.1320470331.
4
Eur J Pediatr. 2007 Feb;166(2):111-6. doi: 10.1007/s00431-006-0295-9. Epub 2006 Nov 8.
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21.
Hum Genet. 1994 Feb;93(2):103-8. doi: 10.1007/BF00210591.
5
Easy calculations of lod scores and genetic risks on small computers.在小型计算机上轻松计算连锁分析计分和遗传风险。
Am J Hum Genet. 1984 Mar;36(2):460-5.
6
Prevalence of left-sided obstructive lesions in patients with atrioventricular canal without Down's syndrome.
J Thorac Cardiovasc Surg. 1986 Mar;91(3):467-9.
7
Atrioventricular canal associated with trisomy 9.与9号染色体三体相关的房室管
Chest. 1989 Dec;96(6):1420-1. doi: 10.1378/chest.96.6.1420.
8
Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome.
Am J Dis Child. 1990 Oct;144(10):1120-2. doi: 10.1001/archpedi.1990.02150340066025.
9
[Trisomy 18 associated with atrioventricular canal].[18三体综合征合并房室通道]
G Ital Cardiol. 1991 Apr;21(4):433-5.
10
Nonrandom association of atrioventricular canal and del (8p) syndrome.房室管与8号染色体短臂缺失（del(8p)）综合征的非随机关联。
Am J Med Genet. 1992 Feb 15;42(4):424-7. doi: 10.1002/ajmg.1320420404.