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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 30, 2024
De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity
Marine Tessarech, Gaëlle Friocourt, Florent Marguet, et al.
European Journal of Human Genetics : EJHG
|
September 22, 2025
Further phenotypical delineation of DLG3-related neurodevelopmental disorders
Marlène Malbos, Thierry Gautier, Amelle Shillington, et al.
Neurology. Genetics
|
December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathy
Nancy Vegas, Mara Cavallin, Camille Maillard, et al.
Human Mutation
|
November 3, 2011
Novel comprehensive diagnostic strategy in Pitt-Hopkins syndrome: clinical score and further delineation of the TCF4 mutational spectrum
Sandra Whalen, Delphine Héron, Thierry Gaillon, et al.
Pediatric Neurology
|
August 24, 2024
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder
Maria Carla Borroto, Heena Patel, Siddharth Srivastava, et al.
Clinical Genetics
|
February 29, 2024
Cerebral dural arteriovenous fistulas in patients with PTEN-related hamartoma tumor syndrome
Anna Gerasimenko, Cyril Mignot, Olivier Naggara, et al.
Plos Genetics
|
December 1, 2018
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, et al.
Epilepsia
|
September 30, 2024
POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia
Joseph D Symonds, Kristen L Park, Cyril Mignot, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2021
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
Sandra Whalen, Marie Shaw, Cyril Mignot, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11
Alice Goldenberg, Florence Riccardi, Aude Tessier, et al.
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Search research articles
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Showing results (111-120 of 216) with videos related to
Sort By:
Page
of 22
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 30, 2024
De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity
Marine Tessarech, Gaëlle Friocourt, Florent Marguet, et al.
European Journal of Human Genetics : EJHG
|
September 22, 2025
Further phenotypical delineation of DLG3-related neurodevelopmental disorders
Marlène Malbos, Thierry Gautier, Amelle Shillington, et al.
Neurology. Genetics
|
December 12, 2018
Delineating <i>FOXG1</i> syndrome: From congenital microcephaly to hyperkinetic encephalopathy
Nancy Vegas, Mara Cavallin, Camille Maillard, et al.
Human Mutation
|
November 3, 2011
Novel comprehensive diagnostic strategy in Pitt-Hopkins syndrome: clinical score and further delineation of the TCF4 mutational spectrum
Sandra Whalen, Delphine Héron, Thierry Gaillon, et al.
Pediatric Neurology
|
August 24, 2024
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder
Maria Carla Borroto, Heena Patel, Siddharth Srivastava, et al.
Clinical Genetics
|
February 29, 2024
Cerebral dural arteriovenous fistulas in patients with PTEN-related hamartoma tumor syndrome
Anna Gerasimenko, Cyril Mignot, Olivier Naggara, et al.
Plos Genetics
|
December 1, 2018
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, et al.
Epilepsia
|
September 30, 2024
POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia
Joseph D Symonds, Kristen L Park, Cyril Mignot, et al.
European Journal of Human Genetics : EJHG
|
February 19, 2021
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
Sandra Whalen, Marie Shaw, Cyril Mignot, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11
Alice Goldenberg, Florence Riccardi, Aude Tessier, et al.
Page
of 22