Literature DB >> 20329145

Familial atrial septal defect of the primum type: a report of four cases in one sibship.

Y K James, M W Thompson, G A Trusler, A S Trimble.   

Abstract

Entities:  

Year:  1968        PMID： 20329145      PMCID： PMC1923861     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN： 0008-4409            Impact factor:   8.262


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  3 in total

1.  A GENETICAL VIEW OF CARDIOVASCULAR DISEASE. THE LEWIS A. CONNER MEMORIAL LECTURE.

Authors:  V A MCKUSICK
Journal:  Circulation       Date:  1964-09       Impact factor: 29.690

2.  Cardiac malformation in mongolism: a prospective study of 184 mongoloid children.

Authors:  R D ROWE; I A UCHIDA
Journal:  Am J Med       Date:  1961-11       Impact factor: 4.965

3.  Familial nature of congenital heart diseases.

Authors:  J J Nora; T C Meyer
Journal:  Pediatrics       Date:  1966-02       Impact factor: 7.124
  3 in total
  6 in total

1.  Congenital heart defects--the risks to offspring.

Authors:  J Burn
Journal:  Arch Dis Child       Date:  1983-12       Impact factor: 3.791

2.  Familial atrial septal defect in a single generation.

Authors:  T J Richer; W J Gallen; D Z Freidberg
Journal:  Br Heart J       Date:  1972-02

3.  Is a shorter atrioventricular septal length an intermediate phenotype in the spectrum of nonsyndromic atrioventricular septal defects?

Authors:  Sonali S Patel; Larry T Mahoney; Trudy L Burns
Journal:  J Am Soc Echocardiogr       Date:  2012-04-25       Impact factor: 5.251

Review 4.  Familial atrioventricular septal defect: possible genetic mechanisms.

Authors:  A Kumar; C A Williams; B E Victorica
Journal:  Br Heart J       Date:  1994-01

5.  A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

Authors:  L Wilson; A Curtis; J R Korenberg; R D Schipper; L Allan; G Chenevix-Trench; A Stephenson; J Goodship; J Burn
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

6.  Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21.

Authors:  A J Cousineau; R M Lauer; M E Pierpont; T L Burns; R H Ardinger; S R Patil; V C Sheffield
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132
  6 in total

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