Additional file 2 of Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families

Autor:	Issa, Mahmoud Y., Zinayida Chechlacz, Stanley, Valentina, George, Renee D., McEvoy-Venneri, Jennifer, Belandres, Denice, Elbendary, Hasnaa M., Gaber, Khaled R., Nabil, Ahmed, Abdel-Hamid, Mohamed S., Zaki, Maha S., Gleeson, Joseph G.
Rok vydání:	2020
DOI:	10.6084/m9.figshare.12299717.v1
Popis:	Additional file 2: Data S1. SimulConsult® Phenome-Genome output pages on each family qualifying for referral for amniocentesis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3409d5838471c162b931855b770908b7 Zobrazit plný text záznamu