Gene-specific PubMed Links (ATRNL1)
2019
Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea
Abstract
Full
2018
Circular RNA CpG island hypermethylation-associated silencing in human cancer
Abstract
Full
2015
Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
Abstract
Full
2015
Identification of atypical ATRNL1 insertion to the EML4-ALK fusion gene in NSCLC.
Abstract
2010
De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features.
Abstract
2007
Genetic analysis of attractin homologs.
Abstract
2004
Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries
Abstract
Full
2003
Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein
Abstract
Full
1998
Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins
Abstract
Full
Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea
Abstract
Full
2018
Circular RNA CpG island hypermethylation-associated silencing in human cancer
Abstract
Full
2015
Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
Abstract
Full
2015
Identification of atypical ATRNL1 insertion to the EML4-ALK fusion gene in NSCLC.
Abstract
2010
De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features.
Abstract
2007
Genetic analysis of attractin homologs.
Abstract
2004
Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries
Abstract
Full
2003
Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein
Abstract
Full
1998
Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins
Abstract
Full