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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
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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
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Review
2012
Review
2012
Purpose:To evaluate the growth, development, and medical histories of children with short-chain acyl-CoA dehydrogenase and… Expand
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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
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Review
2002
Review
2002
There is consistent evidence that the principal etiology of schizophrenia involves predisposing genetic factors. Recent years… Expand
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