FIRST-TRIMESTER PREDICTION IN FETUS AT RISK FOR MYOTONIC DYSTROPHY
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
1. The apolipoprotein CII gene: Subchromosomal localisation and linkage to the myotonic dystrophy locus;Shaw;Hum Genet,1985
2. Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19;Naylor;Cytogenet Cell Genet,1985
3. Prenatal diagnosis of myotonic dystrophy;Schrott;Clin Genet,1973
4. Prenatal prediction of myotonic dystrophy;Insley;Lancet,1976
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1. Distrofia miotónica de steinert y gestación;Clínica e Investigación en Ginecología y Obstetricia;2003-01
2. Genetic prenatal and preimplantation diagnosis of trinucleotide repeat disorders;Expert Review of Neurotherapeutics;2002-07
3. Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy;Muscle & Nerve;1991-05
4. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers;Japanese journal of human genetics;1989-09
5. Myotonic Dystrophy: Linkage with Apolipoprotein E and Estimation of the Gene Carrier Status with Genetic Markers;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;1989-02
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