Search research articles
Contact Us
Filters
Showing results (541-550 of 915) with videos related to
Page
of 92
Sort By:
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Journal of Neurodevelopmental Disorders
|
April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
Veronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.
Blood
|
December 3, 1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders
K Döhner, J Brown, U Hehmann, et al.
American Journal of Medical Genetics. Part A
|
October 31, 2009
Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome
Shin-Ichi Horike, Jose Carlos P Ferreira, Makiko Meguro-Horike, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
June 24, 2014
Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants
Joanna Martin, Miriam Cooper, Marian L Hamshere, et al.
Journal of Medical Genetics
|
April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome
L Bentley, K Nakabayashi, D Monk, et al.
International Psychogeriatrics
|
October 31, 2013
Effect of methylphenidate on attention in apathetic AD patients in a randomized, placebo-controlled trial
Krista L Lanctôt, Sarah A Chau, Nathan Herrmann, et al.
Biomolecules
|
May 24, 2024
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes
Leo McKay, Berardino Petrelli, Molly Pind, et al.
Pediatrics
|
December 20, 2015
Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic Autism
Andreas Schulze, Margaret Bauman, Anne Chun-Hui Tsai, et al.
American Journal of Medical Genetics. Part A
|
September 13, 2017
HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia
Sandra A Farrell, Sandi Sodhi, Christian R Marshall, et al.
Page
of 92
Search research articles
Search
Showing results (541-550 of 915) with videos related to
Sort By:
Page
of 92
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Journal of Neurodevelopmental Disorders
|
April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
Veronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.
Blood
|
December 3, 1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders
K Döhner, J Brown, U Hehmann, et al.
American Journal of Medical Genetics. Part A
|
October 31, 2009
Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome
Shin-Ichi Horike, Jose Carlos P Ferreira, Makiko Meguro-Horike, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
June 24, 2014
Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants
Joanna Martin, Miriam Cooper, Marian L Hamshere, et al.
Journal of Medical Genetics
|
April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome
L Bentley, K Nakabayashi, D Monk, et al.
International Psychogeriatrics
|
October 31, 2013
Effect of methylphenidate on attention in apathetic AD patients in a randomized, placebo-controlled trial
Krista L Lanctôt, Sarah A Chau, Nathan Herrmann, et al.
Biomolecules
|
May 24, 2024
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes
Leo McKay, Berardino Petrelli, Molly Pind, et al.
Pediatrics
|
December 20, 2015
Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic Autism
Andreas Schulze, Margaret Bauman, Anne Chun-Hui Tsai, et al.
American Journal of Medical Genetics. Part A
|
September 13, 2017
HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia
Sandra A Farrell, Sandi Sodhi, Christian R Marshall, et al.
Page
of 92