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22q11.2 deletion syndrome (22q) is a chromosome disorder, where a segment of chromosome 22, located at q11.2, is… Expand Case A 46-year-old man presented to the Emergency Department following a seizure. He had a low serum calcium level of 1.94mmol/L… Expand Background: Patients with 22q deletion syndrome are at increased risk of submucous cleft palate and velopharyngeal insufficiency… Expand Purpose:To evaluate the growth, development, and medical histories of children with short-chain acyl-CoA dehydrogenase and… Expand Adoptive transfer of mature T cells (ATMTC) through bone marrow (BM) transplantation, first attempted over 20 years ago, has… Expand Current clinical and research neuroimaging protocols acquire images using multiple modalities, for instance, T1, T2, diffusion… Expand OBJECTIVE
Cryptic subtelomeric chromosome rearrangements account for 6% to 10% of idiopathic mental retardation. As cytogenetic… Expand There is consistent evidence that the principal etiology of schizophrenia involves predisposing genetic factors. Recent years… Expand The proband was the first child of a young, healthy and non-consanguineous couple. The family history was unremarkable. The… Expand