Prenatal diagnosis of neurofibromatosis type 1: From flanking rflps to intragenic microsatellite markers
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference27 articles.
1. A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]
2. A highly polymorphic cDNA probe in theNF1gene
3. A compound nucleotide repeat in the neurofibro-matosis (NF1) gene
4. Mspl RFLP at CRYB1 locus (17q11.2 – 17q12)
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1. Prenatal Testing for Variants in Genes Associated with Hereditary Cancer Risk;The Journal of Molecular Diagnostics;2024-03
2. Tumor LOH analysis provides reliable linkage information for prenatal genetic testing of sporadic NF1 patients;Genes, Chromosomes and Cancer;2007-09
3. Neurofibromatosis 1: Analysis of the demand for prenatal diagnosis in a French cohort of 361 patients;American Journal of Medical Genetics Part A;2007
4. Review Article : NF1 Mutations and Molecular Testing;Journal of Child Neurology;2002-08
5. Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation;PRENATAL DIAG;1999
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