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Kristin Barañano

Showing results (1-10 of 7) with videos related to

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Maternal Health, Neonatology and Perinatology|January 18, 2022
CNS Malformations in the NewbornKristin Barañano, Irina Burd
Neurogenetics|January 12, 2018
Monogenic disorders that mimic the phenotype of Rett syndromeSiddharth Srivastava, Sonal Desai, Julie Cohen, et al.
Annals of Neurology|August 19, 2014
Clinical whole exome sequencing in child neurology practiceSiddharth Srivastava, Julie S Cohen, Hilary Vernon, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsyLeah Fleming, Monica Lemmon, Natalie Beck, et al.
American Journal of Medical Genetics. Part A|July 29, 2024
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018Antonie D Kline, Ian D Krantz, Masashige Bando, et al.
American Journal of Human Genetics|April 19, 2016
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 DeletionsBrieana Fregeau, Bum Jun Kim, Andrés Hernández-García, et al.
Human Mutation|February 10, 2021
TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical developmentGeeske M van Woerden, Melanie Bos, Charlotte de Konink, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Maternal Health, Neonatology and Perinatology|January 18, 2022
CNS Malformations in the NewbornKristin Barañano, Irina Burd
Neurogenetics|January 12, 2018
Monogenic disorders that mimic the phenotype of Rett syndromeSiddharth Srivastava, Sonal Desai, Julie Cohen, et al.
Annals of Neurology|August 19, 2014
Clinical whole exome sequencing in child neurology practiceSiddharth Srivastava, Julie S Cohen, Hilary Vernon, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsyLeah Fleming, Monica Lemmon, Natalie Beck, et al.
American Journal of Medical Genetics. Part A|July 29, 2024
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018Antonie D Kline, Ian D Krantz, Masashige Bando, et al.
American Journal of Human Genetics|April 19, 2016
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 DeletionsBrieana Fregeau, Bum Jun Kim, Andrés Hernández-García, et al.
Human Mutation|February 10, 2021
TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical developmentGeeske M van Woerden, Melanie Bos, Charlotte de Konink, et al.
Pageof 1