Krishnamurthy N, Krishna D, Sanjana , Rathinasamy J, Kumar A, Francis A
Glob Med Genet. 2025; 12(1):100008.
PMID: 39925442
PMC: 11800308.
DOI: 10.1016/j.gmg.2024.100008.
Bertini V, Cambi F, Legitimo A, Costagliola G, Consolini R, Valetto A
Genes (Basel). 2025; 16(1).
PMID: 39858619
PMC: 11764475.
DOI: 10.3390/genes16010072.
Shima H, Miura A, Kawashima S, Umeki I, Sogi C, Suzuki D
Clin Pediatr Endocrinol. 2025; 34(1):54-59.
PMID: 39777126
PMC: 11701020.
DOI: 10.1297/cpe.2024-0024.
Sun C, Han P, Yan J
Cent Eur J Immunol. 2024; 49(3):315-319.
PMID: 39720268
PMC: 11664810.
DOI: 10.5114/ceji.2024.143229.
Jafar B, Alemayehu H, Bhat R, Zayek M
J Pediatr Genet. 2024; 13(3):237-244.
PMID: 39086451
PMC: 11288709.
DOI: 10.1055/s-0042-1750748.
Genetic profile of a large Spanish cohort with hypercalcemia.
Garcia-Castano A, Madariaga L, Gomez-Conde S, Gonzalez P, Grau G, Rica I
Front Endocrinol (Lausanne). 2024; 15:1297614.
PMID: 38586466
PMC: 10998451.
DOI: 10.3389/fendo.2024.1297614.
Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?.
Manero-Azua A, Pereda A, Llano-Rivas I, Garin I, Perez de Nanclares G
Front Genet. 2023; 14:1274056.
PMID: 37854056
PMC: 10580081.
DOI: 10.3389/fgene.2023.1274056.
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach.
Szczawinska-Poplonyk A, Schwartzmann E, Chmara Z, Glukowska A, Krysa T, Majchrzycki M
Int J Mol Sci. 2023; 24(9).
PMID: 37176024
PMC: 10179617.
DOI: 10.3390/ijms24098317.
A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion.
Paranjape N, Lin Y, Flores-Ramirez Q, Sarin V, Johnson A, Chu J
Sci Rep. 2023; 13(1):7689.
PMID: 37169815
PMC: 10175260.
DOI: 10.1038/s41598-023-34325-2.
Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting.
Saia F, Prato A, Saccuzzo L, Madia F, Barone R, Fichera M
Genes (Basel). 2023; 14(2).
PMID: 36833427
PMC: 9956985.
DOI: 10.3390/genes14020500.
Case report: Late middle-aged features of variant, Kenny-Caffey syndrome type 2-suggestive symptoms during a long follow-up.
Ohmachi Y, Urai S, Bando H, Yokoi J, Yamamoto M, Kanie K
Front Endocrinol (Lausanne). 2023; 13:1073173.
PMID: 36686468
PMC: 9846794.
DOI: 10.3389/fendo.2022.1073173.
Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.
Mustillo P, Sullivan K, Chinn I, Notarangelo L, Haddad E, Davies E
J Clin Immunol. 2023; 43(2):247-270.
PMID: 36648576
PMC: 9892161.
DOI: 10.1007/s10875-022-01418-y.
Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect.
Zemet R, Krispin E, Johnson R, Kumar N, Westerfield L, Stover S
Ultrasound Obstet Gynecol. 2023; 61(6):719-727.
PMID: 36610024
PMC: 10238557.
DOI: 10.1002/uog.26152.
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study.
Putotto C, Pulvirenti F, Pugnaloni F, Isufi I, Unolt M, Anaclerio S
Genes (Basel). 2022; 13(12).
PMID: 36553601
PMC: 9778342.
DOI: 10.3390/genes13122334.
The 22q11.2 Low Copy Repeats.
Vervoort L, Vermeesch J
Genes (Basel). 2022; 13(11).
PMID: 36421776
PMC: 9690962.
DOI: 10.3390/genes13112101.
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Gavril E, Popescu R, Nuca I, Ciobanu C, Butnariu L, Rusu C
Genes (Basel). 2022; 13(11).
PMID: 36360320
PMC: 9690028.
DOI: 10.3390/genes13112083.
Copy number variants and fetal growth in stillbirths.
Dalton S, Workalemahu T, Allshouse A, Page J, Reddy U, Saade G
Am J Obstet Gynecol. 2022; 228(5):579.e1-579.e11.
PMID: 36356697
PMC: 10149588.
DOI: 10.1016/j.ajog.2022.11.1274.
Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort.
Lengyel A, Pinti E, Piko H, Kristof A, Abonyi T, Nemethi Z
Mol Cytogenet. 2022; 15(1):47.
PMID: 36320065
PMC: 9623912.
DOI: 10.1186/s13039-022-00623-z.
Case Report: Chinese female patients with a heterozygous pathogenic gene variant c.898C>T and distal 22q11.2 microdeletion.
Cong Y, Jin H, Wu K, Wang H, Wang D
Front Genet. 2022; 13:900226.
PMID: 36046249
PMC: 9420874.
DOI: 10.3389/fgene.2022.900226.
Copy number variants and placental abnormalities in stillborn fetuses: A secondary analysis of the Stillbirth Collaborative Research Network study.
Workalemahu T, Dalton S, Allshouse A, Carey A, Page J, Blue N
BJOG. 2022; 129(13):2125-2131.
PMID: 35876766
PMC: 9643668.
DOI: 10.1111/1471-0528.17269.