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CROSS-SECTIONAL AND LONGITUDINAL CHARACTERISATION OF THE DEVELOPMENTAL PHENOTYPE IN (22)Q(11.2) DUPLICATION

Collaboration of perioperative management in an adult patient with 22 q 11.2 deletion syndrome: A case

Extinction in the 11.2 mu m PAH band and the low L-11.2/L-IR in ULIRGs

22q11.2 deletion detected by in situ hybridization in 22/39 Mexican patients with velocardiofacial syndrome-like

Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism

Covering groups of M-22 as regular Galois groups over Q

The (p, q, r)-Generations of the Mathieu Group M-22

A 128 Gb/s, 11.2 mW Single-Ended PAM4 Linear TIA With 2.7 mu ${A}_{{rms}}}$ Input Noise in 22 nm FinFET

Xp 11.2 translocation: the challenge in a diagnosis

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome

Monocrystalline 1.7-eV-Bandgap MgCdTe Solar Cell With 11.2% Efficiency

High-precision Q(EC)-value measurement of the superallowed beta(+) emitter Mg-22 and an ab initio evaluationof the A=22 isobaric triplet

Truncus arteriosus survival outcomes: Does 22q 11.2 deletion matter?

Mosaicism in 22q11.2 Microdeletion Syndrome

22q11.2 deletion syndrome and schizophrenia

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