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UnknownPrevention of delayed nausea: a University of Rochester Cancer Center Community Clinical Oncology Program study of patients receiving chemotherapy.
Not available
S-EPMC3438235 | biostudies-literature
UnknownCopy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Not available
S-EPMC4570279 | biostudies-literature
UnknownVariance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.
Not available
S-EPMC6209529 | biostudies-literature
UnknowniDiabetes platform-enhanced phenotyping of patients with diabetes for precision diagnosis, prognosis and treatment: study protocol for a cluster-randomised controlled study in Tayside, Scotland.
Not available
S-EPMC11605812 | biostudies-literature
UnknownA normative chart for cognitive development in a genetically selected population.
Not available
S-EPMC9117666 | biostudies-literature
UnknownEnhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Not available
S-EPMC3591861 | biostudies-literature
UnknownGenome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Not available
S-EPMC5647121 | biostudies-literature
UnknownComplete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Not available
S-EPMC7077921 | biostudies-literature
UnknownEffect of alteplase on the CT hyperdense artery sign and outcome after ischemic stroke.
Not available
S-EPMC4731690 | biostudies-literature
UnknownPractical guidelines for managing patients with 22q11.2 deletion syndrome.
Not available
S-EPMC3197829 | biostudies-literature
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