Literature DB >> 14044319

CHROMOSOME STUDIES IN PATIENTS WITH SUPRAVALVULAR AORTIC STENOSIS.

P EBERLE, A J BEUREN.   

Abstract

Entities:  

Keywords:  AORTIC VALVE STENOSIS; CHROMOSOME ABNORMALITIES; GENETICS, HUMAN

Mesh:

Year:  1963        PMID: 14044319     DOI: 10.1016/s0140-6736(63)92177-9

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  8 in total

1.  FAMILIAL SUPRAVALVAR AORTIC STENOSIS.

Authors:  W F LOGAN; E W JONES; E WALKER; N COULSHED; E J EPSTEIN
Journal:  Br Heart J       Date:  1965-07

2.  Pulmonary valvular dysplasia. A cardiofacial syndrome.

Authors:  L M Linde; S W Turner; R S Sparkes
Journal:  Br Heart J       Date:  1973-03

3.  Chromosome studies in 156 patients with congenital heart disease.

Authors:  J M Anders; E C Moores; R Emanuel
Journal:  Br Heart J       Date:  1965-09

4.  Causes of malformations of the heart.

Authors: 
Journal:  Br Med J       Date:  1965-10-16

Review 5.  Williams syndrome.

Authors:  J Burn
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

6.  Unbalanced 13;18 translocation and Williams syndrome.

Authors:  A Colley; Y Thakker; H Ward; D Donnai
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

7.  [Genetic studies in supravalvular aortic stenoses].

Authors:  G Jörgensen; A J Beuren
Journal:  Humangenetik       Date:  1965

8.  Idiopathic infantile hypercalcaemia--a continuing enigma.

Authors:  N D Martin; G J Snodgrass; R D Cohen
Journal:  Arch Dis Child       Date:  1984-07       Impact factor: 3.791

  8 in total

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