• Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome
• ATR regulates neuronal activity by modulating presynaptic firing
• CtIP Mutations Cause Seckel and Jawad Syndromes
• Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
• Functional interplay between the oxidative stress response and DNA damage checkpoint signaling for genome maintenance in aerobic organisms
• Genetic and congenital disorders in pre-Hispanic Moche pottery
• Insights on cross-species transmission of SARS-CoV-2 from structural modeling
• Insights on cross-species transmission of SARS-CoV-2 from structural modeling
• Intracranial aneurysms in microcephalic primordial dwarfism: a systematic review
• Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in <em>RTTN</em> Gene: A Seckel Syndrome Case Report
• Modifier Genes in Microcephaly: A Report on <em>WDR62</em>, <em>CEP63</em>, <em>RAD50</em> and <em>PCNT</em> Variants Exacerbating Disease Caused by Biallelic Mutations of <em>ASPM</em> and <e
• Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families
• Nephrolithiasis in a 17-Year-Old Male With Seckel Syndrome and Horseshoe Kidneys: Case Report and Review of the Literature
• Prenatal diagnosis of Seckel syndrome at 21 weeks' gestation and review of the literature
• Primary Dwarfism, Microcephaly, and Chorioretinopathy due to a PLK4 Mutation in Two Siblings
• Pulmonary hypertensive crisis: A potential reason for right ventricle and pacemaker lead failure
• Siblings Seckel's syndrome 1 caused by ATR gene variants in a sibpair
• The shortest of the short: pericentrin mutations and beyond
• Visual vignette. Seckel syndrome