Maternal Consequences of the Detection of Fragile X Carriers in Newborn Screening

OBJECTIVES: The possibility of newborn screening for fragile X syndrome is complicated by the potential for identifying premutation carriers. Although knowing the child’s carrier status has potential benefits, the possibility of late-onset disorders in carrier children and their parents raises conce...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Pediatrics
Egile Nagusiak: Bailey, Donald B., Wheeler, Anne, Berry-Kravis, Elizabeth, Hagerman, Randi, Tassone, Flora, Powell, Cynthia M., Roche, Myra, Gane, Louise W., Sideris, John
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Academy of Pediatrics 2015
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4516945/
https://ncbi.nlm.nih.gov/pubmed/26169437
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2015-0414
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