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
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2018

Circular RNA CpG island hypermethylation-associated silencing in human cancer
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2015

Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
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2015

Identification of atypical ATRNL1 insertion to the EML4-ALK fusion gene in NSCLC.
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2010

De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features.
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2007

Genetic analysis of attractin homologs.
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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
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2003

Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein
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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
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