Search research articles
Contact Us
Filters
Showing results (1-10 of 29) with videos related to
Page
of 3
Sort By:
Clinical Genetics
|
March 21, 2002
HotSpots
M E Suzanne Lewis
Genes
|
December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> Variant
Silas Yip, Kristina Calli, Ying Qiao, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique
|
August 5, 2005
Addressing health disparities through promoting equity for individuals with intellectual disability
Hélène Ouellette-Kuntz, Nathalie Garcin, M E Suzanne Lewis, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2007
Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3
William T Gibson, Chansonette Harvard, Ying Qiao, et al.
BMC Medical Genetics
|
November 12, 2016
Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication
Jila Dastan, Chieko Chijiwa, Flamingo Tang, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2005
Systemic lupus erythematosus and other autoimmune disorders in children with Noonan syndrome
Elena Lopez-Rangel, Peter N Malleson, David S Lirenman, et al.
Journal of Autism and Developmental Disorders
|
January 12, 2007
Trends in special education code assignment for autism: implications for prevalence estimates
Hélène Ouellette-Kuntz, Helen Coo, Jennifer E V Lloyd, et al.
Journal of Autism and Developmental Disorders
|
November 3, 2007
Trends in autism prevalence: diagnostic substitution revisited
Helen Coo, Hélène Ouellette-Kuntz, Jennifer E V Lloyd, et al.
Journal of Autism and Developmental Disorders
|
November 12, 2010
Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families
Xudong Liu, Fatima Solehdin, Ira L Cohen, et al.
Pediatric Research
|
March 26, 2021
Tackling healthcare access barriers for individuals with autism from diagnosis to adulthood
Natasha Malik-Soni, Andrew Shaker, Helen Luck, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Clinical Genetics
|
March 21, 2002
HotSpots
M E Suzanne Lewis
Genes
|
December 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> Variant
Silas Yip, Kristina Calli, Ying Qiao, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique
|
August 5, 2005
Addressing health disparities through promoting equity for individuals with intellectual disability
Hélène Ouellette-Kuntz, Nathalie Garcin, M E Suzanne Lewis, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2007
Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3
William T Gibson, Chansonette Harvard, Ying Qiao, et al.
BMC Medical Genetics
|
November 12, 2016
Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication
Jila Dastan, Chieko Chijiwa, Flamingo Tang, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2005
Systemic lupus erythematosus and other autoimmune disorders in children with Noonan syndrome
Elena Lopez-Rangel, Peter N Malleson, David S Lirenman, et al.
Journal of Autism and Developmental Disorders
|
January 12, 2007
Trends in special education code assignment for autism: implications for prevalence estimates
Hélène Ouellette-Kuntz, Helen Coo, Jennifer E V Lloyd, et al.
Journal of Autism and Developmental Disorders
|
November 3, 2007
Trends in autism prevalence: diagnostic substitution revisited
Helen Coo, Hélène Ouellette-Kuntz, Jennifer E V Lloyd, et al.
Journal of Autism and Developmental Disorders
|
November 12, 2010
Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families
Xudong Liu, Fatima Solehdin, Ira L Cohen, et al.
Pediatric Research
|
March 26, 2021
Tackling healthcare access barriers for individuals with autism from diagnosis to adulthood
Natasha Malik-Soni, Andrew Shaker, Helen Luck, et al.
Page
of 3