Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marta Sánchez-Delgado"'
Autor:
Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, Jose Ramon Hernandez Mora, Nuria Tubío Santamaría, Eduard Gratacós, Manel Esteller, Miguel López de Heredia, Virgina Nunes, Cecile Choux, Patricia Fauque, Guiomar Perez de Nanclares, Lauren Anton, Michal A. Elovitz, Isabel Iglesias-Platas, David Monk
Publikováno v:
Clinical Epigenetics, Vol 11, Iss 1, Pp 1-15 (2019)
Abstract Background Genome-wide studies have begun to link subtle variations in both allelic DNA methylation and parent-of-origin genetic effects with early development. Numerous reports have highlighted that the placenta plays a critical role in coo
Externí odkaz:
https://doaj.org/article/9d5ca46d9ac84d09bb6127d3c0d24f71
Autor:
Montserrat Milà, David Monk, Francisco Martínez, Zeynep Tümer, Marta Sánchez Delgado, Cristina Camprubí
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 165:472-478
The phenotype overlap between autism spectrum disorders (ASD) & intellectual disabilities (ID) is mirrored at the genetic level, with common genes being reported mutated in variety of developmental disabilities. However despite widespread genetic scr
Autor:
Sabria-Back, Joan, Monteagudo-Sášnchez, Ana, Sa'nchez-Delgado, Marta, Ferguson-Smith, Anne C., Gómez, Olga, Cartada, Africa Pertierra, Tenorio, Jair, Nevado, Julián, Lapunzina, Pablo, Aguirre, Arrate Pereda, Sevilla, Carles Giménez, Toro, Estefanía Toro, de Nanclares, Guiomar Perez, Monk, David
Publikováno v:
Journal of Medical Genetics; Mar2022, Vol. 59 Issue 3, p253-261, 13p
Autor:
Monteagudo-Sánchez, Ana1 amonteagudo@idibell.cat, Sánchez-Delgado, Marta1 marta.sanchezdel@gmail.com, Mora, Jose Ramon Hernandez1 jhernandezm@idibell.cat, Santamaría, Nuria Tubío1,2 nuria.tubiosantamaria@gmail.com, Gratacós, Eduard3 egratacos@sjdhospitalbarcelona.org, Esteller, Manel4,5,6 mesteller@idibell.cat, de Heredia, Miguel López7 mlopezheredia@idibell.cat, Nunes, Virgina5,7,8 vnunes@idibell.cat, Choux, Cecile9 cecile.choux@gmail.com, Fauque, Patricia9 patricia.fauque@chu-dijon.fr, de Nanclares, Guiomar Perez10 guiomar.perezdenanclaresleal@osakidetza.eus, Anton, Lauren11 lanton@pennmedicine.upenn.edu, Elovitz, Michal A.11 melovitz@obgyn.upenn.edu, Iglesias-Platas, Isabel12 isa0iglesias@hotmail.com, Monk, David1 dmonk@idibell.cat
Publikováno v:
Clinical Epigenetics. 2/26/2019, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p.
Autor:
Delgado, Marta Sánchez, Camprubí, Cristina, Tümer, Zeynep, Martínez, Francisco, Milà, Montserrat, Monk, David
Publikováno v:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics; Sep2014, Vol. 165B Issue 6, p472-478, 7p
Autor:
Carlos Simón, Carmen Rubio
Different genetic diagnostic and treatment options are used worldwide to improve routine IVF procedures for the benefit of patients. This handbook updates the new genetic diagnostic technologies that have been translated to the clinic, aiming to impr