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22q deletion syndrome

Known as: 22q- syndrome 
National Institutes of Health

Papers overview

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2020
2020
BACKGROUND 22q11.2 deletion syndrome (22q) is a chromosome disorder, where a segment of chromosome 22, located at q11.2, is… Expand
2015
2015
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
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Review
2012
Review
2012
Background: Patients with 22q deletion syndrome are at increased risk of submucous cleft palate and velopharyngeal insufficiency… Expand
Review
2012
Review
2012
Purpose:To evaluate the growth, development, and medical histories of children with short-chain acyl-CoA dehydrogenase and… Expand
2009
2009
Adoptive transfer of mature T cells (ATMTC) through bone marrow (BM) transplantation, first attempted over 20 years ago, has… Expand
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2007
2007
Current clinical and research neuroimaging protocols acquire images using multiple modalities, for instance, T1, T2, diffusion… Expand
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Highly Cited
2004
Highly Cited
2004
OBJECTIVE Cryptic subtelomeric chromosome rearrangements account for 6% to 10% of idiopathic mental retardation. As cytogenetic… Expand
Review
2002
Review
2002
There is consistent evidence that the principal etiology of schizophrenia involves predisposing genetic factors. Recent years… Expand
1998
1998
The proband was the first child of a young, healthy and non-consanguineous couple. The family history was unremarkable. The… Expand