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Current Opinion in Neurology
|
April 20, 2004
Eye movements in neurodevelopmental disorders
John A Sweeney, Yukari Takarae, Carol Macmillan, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2017
De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome
Angela Sagar, Dalila Pinto, Fedra Najjar, et al.
American Journal of Medical Genetics. Part A
|
November 16, 2019
Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study
Erin K Bojanek, Matthew W Mosconi, Stephen Guter, et al.
Applied Neuropsychology
|
March 17, 2007
Effects of polymorphisms of chemokine receptors on neurodevelopment and the onset of encephalopathy in children with perinatal HIV-1 infection
Antolin Llorente, Pim Brouwers, Bruce Thompson, et al.
Archives of General Psychiatry
|
August 4, 2010
Neurobehavioral abnormalities in first-degree relatives of individuals with autism
Matthew W Mosconi, Margaret Kay, Anna-Maria D'Cruz, et al.
American Journal of Human Genetics
|
June 15, 2005
A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians
Anne-Marie Laberge, Michele Jomphe, Louis Houde, et al.
American Journal of Medical Genetics. Part A
|
September 13, 2021
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin
Charlotte von der Lippe, Kristian Tveten, Trine E Prescott, et al.
American Journal of Human Genetics
|
March 7, 2020
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
Lucia V Schottlaender, Rosella Abeti, Zane Jaunmuktane, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Current Opinion in Neurology
|
April 20, 2004
Eye movements in neurodevelopmental disorders
John A Sweeney, Yukari Takarae, Carol Macmillan, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2017
De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome
Angela Sagar, Dalila Pinto, Fedra Najjar, et al.
American Journal of Medical Genetics. Part A
|
November 16, 2019
Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study
Erin K Bojanek, Matthew W Mosconi, Stephen Guter, et al.
Applied Neuropsychology
|
March 17, 2007
Effects of polymorphisms of chemokine receptors on neurodevelopment and the onset of encephalopathy in children with perinatal HIV-1 infection
Antolin Llorente, Pim Brouwers, Bruce Thompson, et al.
Archives of General Psychiatry
|
August 4, 2010
Neurobehavioral abnormalities in first-degree relatives of individuals with autism
Matthew W Mosconi, Margaret Kay, Anna-Maria D'Cruz, et al.
American Journal of Human Genetics
|
June 15, 2005
A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians
Anne-Marie Laberge, Michele Jomphe, Louis Houde, et al.
American Journal of Medical Genetics. Part A
|
September 13, 2021
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin
Charlotte von der Lippe, Kristian Tveten, Trine E Prescott, et al.
American Journal of Human Genetics
|
March 7, 2020
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
Lucia V Schottlaender, Rosella Abeti, Zane Jaunmuktane, et al.
Page
of 1