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Isaac Kearney's mum regularly posts updates to social media about her son's love for Liverpool Football Club and the players.
Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access information on a device and to provide personalised ads and content, ad and ...
For the new study, Dr. Worobey, Dr. Pekar and their colleagues compared the genomes of 250 coronaviruses, using their genetic similarities and differences to determine their relationships.
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Justdial on MSNApert Syndrome: Causes, Symptoms, Diagnosis and TreatmentLearn all about Apert Syndrome, its causes, symptoms, diagnosis methods, and treatment options to manage this rare genetic disorder effectively. Read more ...
Craniosynostosis is a birth defect in which the bones in a baby's skull fuse together too early. It requires early diagnosis and treatment.
Metopic craniosynostosis is a rare condition in infants in which the metopic suture, a part of the skull, ... However, it may result from both genetic and environmental factors.
Craniosynostosis is the early fusion of the cranial sutures, which poses numerous diagnostic and medical complications. It is a frequent abnormality that affects 3–5 out of every 10,000 babies.
Boyadjiev SA, International Craniosynostosis C. Genetic analysis of non-syndromic craniosynostosis. Orthod Craniofac Res (2007) 10:129–37. doi: 10.1111/j.1601-6343.2007.00393.x PubMed Abstract | ...
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