Literature DB >> 20084248

Genetics and the canadian paediatric surveillance program.

A Summers1.   

Abstract

Year:  2001        PMID： 20084248      PMCID： PMC2804557          DOI： 10.1093/pch/6.5.269

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN： 1205-7088            Impact factor:   2.253


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  5 in total

Review 1.  CHARGE syndrome: report of 47 cases and review.

Authors:  A L Tellier; V Cormier-Daire; V Abadie; J Amiel; S Sigaudy; D Bonnet; P de Lonlay-Debeney; M P Morrisseau-Durand; P Hubert; J L Michel; D Jan; H Dollfus; C Baumann; P Labrune; D Lacombe; N Philip; M LeMerrer; M L Briard; A Munnich; S Lyonnet
Journal:  Am J Med Genet       Date:  1998-04-13

Review 2.  The Smith-Lemli-Opitz syndrome.

Authors:  R I Kelley; R C Hennekam
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

Review 3.  Biochemical and genetic aspects of 7-dehydrocholesterol reductase and Smith-Lemli-Opitz syndrome.

Authors:  H R Waterham; R J Wanders
Journal:  Biochim Biophys Acta       Date:  2000-12-15

Review 4.  Prenatal diagnosis of Smith-Lemli-Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex-reversed fetus.

Authors:  D P Bick; D McCorkle; W S Stanley; H J Stern; P Staszak; G D Berkovitz; C M Meyers; R I Kelley
Journal:  Prenat Diagn       Date:  1999-01       Impact factor: 3.050

5.  Deletion in chromosome region 22q11 in a child with CHARGE association.

Authors:  K Devriendt; A Swillen; J P Fryns
Journal:  Clin Genet       Date:  1998-05       Impact factor: 4.438
  5 in total

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