Literature DB >> 7069536

Familial hypercholesterolemia: report of coronary death at age 3 in a homozygous child and prenatal diagnosis in a heterozygous sibling.

V Rose, G Wilson, G Steiner.   

Abstract

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Year:  1982        PMID： 7069536     DOI： 10.1016/s0022-3476(82)80579-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  3 in total

1.  Fatal myocardial infarction at 4.5 years in a case of homozygous familial hypercholesterolaemia.

Authors:  Matthias Gautschi; Mladen Pavlovic; Jean-Marc Nuoffer
Journal:  JIMD Rep       Date:  2011-09-06

2.  Chorionic DNA analysis for the prenatal diagnosis of familial hypercholesterolaemia.

Authors:  D A Coviello; S Bertolini; P Masturzo; M Ghisellini; R Tiozzo; F Zambelli; C Stefanutti; F Torcia; A Pachi; G Ricci
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

3.  Prenatal diagnosis of familial hypercholesterolemia caused by the "Lebanese" mutation at the low density lipoprotein receptor locus.

Authors:  A Reshef; V Meiner; E J Dann; M Granat; E Leitersdorf
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132
  3 in total

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