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Literature DB >> 2359098

Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.

Abstract

We studied the karyotypes of 10 members of a family in whom hypertrophic cardiomyopathy is segregating as an autosomal dominant trait. In all those affected by the disease, a fragile site on the long arm of chromosome 16 was found, expressed with different frequencies, but the unaffected family members did not show this trait.

Entities: Disease

Mesh：

Year: 1990 PMID： 2359098 PMCID： PMC1017132 DOI： 10.1136/jmg.27.6.363

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

14 in total

1. THREE FAMILIES WITH FAMILIAL CARDIOMYOPATHY.

Authors: D L BOYD; M E MISKHIN; P D GENOVES
Journal: Ann Intern Med Date: 1965-09 Impact factor: 25.391

2. Fragile sites update.

Authors: F Hecht
Journal: Cancer Genet Cytogenet Date: 1988-03

3. A simple technique for demonstrating centromeric heterochromatin.

Authors: A T Sumner
Journal: Exp Cell Res Date: 1972-11 Impact factor: 3.905

4. Dominant and recessive modes of inheritance in idiopathic cardiomyopathy.

Authors: R Emanuel; R Withers; K O'Brien
Journal: Lancet Date: 1971-11-13 Impact factor: 79.321

5. Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis.

Authors: C E Clark; W L Henry; S E Epstein
Journal: N Engl J Med Date: 1973-10-04 Impact factor: 91.245

6. Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): ventriculographic and echocardiographic features in 30 patients.

Authors: H Yamaguchi; T Ishimura; S Nishiyama; F Nagasaki; S Nakanishi; F Takatsu; T Nishijo; T Umeda; K Machii
Journal: Am J Cardiol Date: 1979-09 Impact factor: 2.778

Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.

1. THREE FAMILIES WITH FAMILIAL CARDIOMYOPATHY.

2. Fragile sites update.

3. A simple technique for demonstrating centromeric heterochromatin.

4. Dominant and recessive modes of inheritance in idiopathic cardiomyopathy.

5. Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis.

6. Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): ventriculographic and echocardiographic features in 30 patients.

7. Heritable fragile sites in cancer.

8. Cancer chromosome breakpoints and common fragile sites induced by aphidicolin.

9. Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

10. Banded chromosome analysis in patients with treatment-associated acute nonlymphocytic leukemia.

1. The genetics of hypertrophic cardiomyopathy.

Review 2. Molecular basis of hypertrophic and dilated cardiomyopathy.