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Epilepsia, ISSN 0013-9580, 05/2019, Volume 60, Issue 5, pp. 830 - 844
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 04/2014, Volume 7, Issue 1, pp. 27 - 27
MicroRNAs (miRNAs) are key regulators of gene expression, playing important roles in development, homeostasis, and disease. Recent experimental evidence... 
GCP5 | miRNA | Digital anomaly | MIR17HG | Skeletal defects | miR-17 ∼ 92 | Analysis | Genetic aspects | Genetic disorders | Autism | Genotype & phenotype | Hypotheses | Consent | Rodents | Fingers & toes | Families & family life | Gene expression | Patients | Children & youth
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 09/2017, Volume 10, Issue 1, pp. 33 - 6
Background: Homozygous mutations and deletions of the microcephalin gene (MCPH1; OMIM *607117) have been identified as a cause of autosomal recessive primary... 
Microdeletion | MCPH1 gene | Primary microcephaly | GENETICS & HEREDITY | CHROMOSOME CONDENSATION | MUTATIONS | BRAIN | US | Case studies | Complications and side effects | Gene mutations | Genetic aspects | Diagnosis | Microcephaly | Risk factors
Journal Article
Oakland Tribune, ISSN 1068-5936, 06/2009
"This is the first time I'm really experiencing what we do for Good Cents," [Allison Rogers], 8, said about her bagging duties. "Up til now, I just brought... 
Newspaper Article
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