Chromosome 22 Central (@c22central) 's Twitter Profile
Chromosome 22 Central

@c22central

🧬C22C official. Support & info for chromosome 22 disorders. 22q11-, 22q11Dup, Emanuel Syndrome, PMS, 22q13-, Trisomy 22, Cat Eye Syndrome #c22c #genetics🧬

ID: 1277410165122314241

linkhttp://www.c22c.org calendar_today29-06-2020 01:16:01

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Chromosome 22 Central (@c22central) 's Twitter Profile Photo

Presence, severity, and functional associations of incomplete hippocampal inversion in 22q11.2 deletion syndrome pubmed.ncbi.nlm.nih.gov/40288750/ #22q #22q11

Chromosome 22 Central (@c22central) 's Twitter Profile Photo

Assessment of vascular tortuosity in 22q11.2 deletion syndrome using optical coherence tomography angiography pubmed.ncbi.nlm.nih.gov/40254227/ #22q #22q11

Chromosome 22 Central (@c22central) 's Twitter Profile Photo

Brain connectivity shift across puberty may explain autism risk in 22q11.2 deletion syndrome via @psypost psypost.org/brain-connecti… #22q11 #22q #autism

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How does altered function of the hippocampus contribute to the development of psychosis? - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40623620/

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Immunological and clinical characteristics in a cohort of Colombian pediatric patients with 22q11.2 deletion - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40615621/

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A Proposal for Neurocognitive Assessment in Spanish-Speaking Adults With Phelan-McDermid Syndrome: A Case Report - #22q13 #phelanmcdermidsyndrome pubmed.ncbi.nlm.nih.gov/40600073/

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Genome Sequencing Uncovers Additional Findings in Phelan-McDermid Syndrome - #22q13 #phelanmcdermidsyndrome pubmed.ncbi.nlm.nih.gov/40519070/

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Dissecting the Phenotypic Spectrum and Complexity of Movement Disorders in 22q11.2 Deletion Syndrome - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40530538/

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22q11.2 Deletion Syndrome: Cognitive, Visuomotor, and Adaptive Functioning Followed Longitudinally - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40525315/

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Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40501680/

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Healthcare Transition to Adulthood in Patients with 22q11.2 Deletion Syndrome: A Comprehensive Literature Review and Transition Framework - #22q #22q11 pubmed.ncbi.nlm.nih.gov/40223294/

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Oxytocin seals the blood–brain barrier, improving 22q11.2 deletion syndrome trajectories academic.oup.com/brain/article-… #22q #22q11

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Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report publications.aap.org/pediatrics/art… #22q #22q11

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Parental Education Predicts Longitudinal IQ Trajectories in 22q11.2 Deletion Syndrome: A Three‐Cohort European Study - Snihirova - Journal of Intellectual Disability Research - Wiley Online Library onlinelibrary.wiley.com/doi/10.1111/ji… #22q #22q11

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Congenital heart disease in 22q11.2 deletion syndrome: a meta-analysis and systematic review of the literature jmg.bmj.com/content/early/… #22q #22q11

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Influence of Polygenic Risk on Height and BMI in Adults With a 22q11.2 Microdeletion academic.oup.com/jes/article/9/… #22q #22q11

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Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report publications.aap.org/pediatrics/art… #22q #22q11

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Groundbreaking Study Uncovers Link Between Mitochondrial Vulnerability and Neurovascular Function in Neuropsychiatric Disorders bioengineer.org/groundbreaking… #22q