New Research: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product: Rett syndrome is an X-linked dominant, postnatal neurological disorder. Approximately 80–90% of… https://t.co/Vusr
Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product - PubMed https://t.co/4mw6Sl0neU
Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product https://t.co/HefplAYXur https://t.co/MpZM1jbR7L