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1 Ergebnisse
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Variability in Phelan-McDermid Syndrome in a Cohort of 210 ..:
Julián Nevado
;
Sixto García-Miñaúr
;
María Palomares-Bralo
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.652454/full. , 2022
Link:
https://doi.org/10.3389/fgene.2022.652454
RT Journal T1
Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:45e2ed9b52f940b0bd31664eea90cf57&Exemplar=1&LAN=DE A1 Julián Nevado A1 Sixto García-Miñaúr A1 María Palomares-Bralo A1 Elena Vallespín A1 Encarna Guillén-Navarro A1 Jordi Rosell A1 Cristina Bel-Fenellós A1 María Ángeles Mori A1 Montserrat Milá A1 Miguel del Campo A1 Pilar Barrúz A1 Fernando Santos-Simarro A1 Gabriela Obregón A1 Carmen Orellana A1 Harry Pachajoa A1 Jair Antonio Tenorio A1 Enrique Galán A1 Juan C. Cigudosa A1 Angélica Moresco A1 César Saleme A1 Silvia Castillo A1 Elisabeth Gabau A1 Luis Pérez-Jurado A1 Ana Barcia A1 Maria Soledad Martín A1 Elena Mansilla A1 Isabel Vallcorba A1 Pedro García-Murillo A1 Franco Cammarata-Scalisi A1 Natálya Gonçalves Pereira A1 Raquel Blanco-Lago A1 Mercedes Serrano A1 Juan Dario Ortigoza-Escobar A1 Blanca Gener A1 Verónica Adriana Seidel A1 Pilar Tirado A1 Pablo Lapunzina A1 Spanish PMS Working Group A1 Mena Rocío A1 Lleguer Roser A1 Fernández-Montaño Victoria A1 Martín Rubén A1 Fernández Blanca A1 García-Santiago Fé A1 Gómez del Pozo Victoria A1 Peña Carolina A1 Alhambra Norma A1 García Carlos A1 Rodríguez Juan Ramón A1 Martínez-Bermejo Antonio A1 Málaga Ignacio A1 Martínez-Monseny Antonio Federico A1 Armstrong Judith A1 Anticona Jennifer A1 Hernando-Davalillo Cristina A1 San Martí Adrián Alcalá A1 Martorell Loreto A1 Yubero Delia A1 Nunes Tania A1 Callaghan Mar O´ A1 Alonso Xenia A1 Ramos Federico A1 López Jesús Casas A1 López-González Vanesa A1 M Juliana Ballesta A1 Armengol Lluís A1 González-Meneses Antonio A1 Borrego Salud A1 Roselló Mónica A1 Suela Javier A1 Pérez-Granero Ángeles A1 Rodríguez-Revenga Laia PB Frontiers Media S.A. YR 2022 K1 autistic behavior K1 22q13 deletion syndrome K1 Phelan-McDermid syndrome (PMS) K1 SHANK3 K1 subtelomeric deletion syndrome K1 intellectual disabilities (ID) K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2022.652454/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.652454 DO https://doi.org/10.3389/fgene.2022.652454 SF ELIB - SuUB Bremen
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