Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP)-Reference-Cited by-同舟云学术

Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP)

Published:2002 Issue:10 Volume:22 Page:914-916
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Francoual Jeanne,Trioche Pascale,Mokrani Chahnez,Seboui Hassen,Khrouf Na�ma,Chalas Jacqueline,Clement Marina,Capel Liliane,Tachdjian G�rard,Labrune Philippe

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference14 articles.

1. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency

2. Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I

3. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

4. Genetic defects at the UGT1 locus associated with Crigler-Najjar type I disease, including a prenatal diagnosis

5. Prenatal diagnosis for cystic fibrosis using SSCP analysis

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3. UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population;IRAN J BASIC MED SCI;2017

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