Appendix: Prenatal Diagnosis of Additional Miscellaneous Genetic Disorders
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Wiley-Blackwell
Reference208 articles.
1. DAX-1 gene mutations and deletions in Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism;Kinoshita;Hormone Res,1997
2. Prenatal diagnosis of congenital adrenal hypoplasia;Peter;Horm Res,1996
3. Importance of genetic diagnosis of DAX-1 deficiency: example from a large, multigenerational family;Ostermann;Horm Res,2006
4. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family;Neerman-Arbez;Blood,2003
5. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects;Monaldini;Thromb Haemost,2007
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