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For: Koczkowska M, Wierzba J, Śmigiel R, Sąsiadek M, Cabała M, Ślężak R, Iliszko M, Kardaś I, Limon J, Lipska-Ziętkiewicz BS. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome. J Appl Genet 2017;58:93-8. [PMID: 27629806 DOI: 10.1007/s13353-016-0366-1] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Liao H, Liao C, Kao S, Chiang C, Chen Y. Detecting 22q11.2 Deletion Syndrome in Newborns with Low T Cell Receptor Excision Circles from Severe Combined Immunodeficiency Screening. The Journal of Pediatrics 2019;204:219-224.e1. [DOI: 10.1016/j.jpeds.2018.08.072] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
2 Cirillo E, Prencipe MR, Giardino G, Romano R, Scalia G, Genesio R, Nitsch L, Pignata C. Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion. The Journal of Allergy and Clinical Immunology: In Practice 2020;8:3112-20. [DOI: 10.1016/j.jaip.2020.06.051] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Lam JK, Braddock SR, Huddleston CB, Knutsen AP. Coexistent TBX1 mutation and chromosomal 20q13.13-q13.2 duplication in an infant with abnormal T-cell receptor rearrangement circle newborn screening results. Ann Allergy Asthma Immunol 2019;122:222-3. [PMID: 30712578 DOI: 10.1016/j.anai.2018.10.020] [Reference Citation Analysis]
4 Hannan FM, Newey PJ, Whyte MP, Thakker RV. Genetics of Skeletal Disorders. Handb Exp Pharmacol 2020;262:325-51. [PMID: 32166388 DOI: 10.1007/164_2020_350] [Reference Citation Analysis]
5 Gulati A, Dahl N, Tufro A. Inherited glomerular diseases in the gilded age of genomic advancements. Pediatr Nephrol 2020;35:959-68. [PMID: 31049720 DOI: 10.1007/s00467-019-04266-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
6 Logjes RJH, Breugem CC, Van Haaften G, Paes EC, Sperber GH, van den Boogaard MH, Farlie PG. The ontogeny of Robin sequence. Am J Med Genet A 2018;176:1349-68. [PMID: 29696787 DOI: 10.1002/ajmg.a.38718] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 3.8] [Reference Citation Analysis]
7 Sgardioli IC, Paoli Monteiro F, Fanti P, Paiva Vieira T, Gil-da-Silva-Lopes VL. Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health. Orphanet J Rare Dis 2019;14:123. [PMID: 31159889 DOI: 10.1186/s13023-019-1098-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
8 Li S, Jin Y, Yang J, Yang L, Tang P, Zhou C, Wu L, Dong J, Chen J, Shen H. Prenatal diagnosis of rearrangements in the fetal 22q11.2 region. Mol Cytogenet 2020;13:28. [PMID: 32670410 DOI: 10.1186/s13039-020-00498-y] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
9 Hannan FM, Newey PJ, Whyte MP, Thakker RV. Genetic approaches to metabolic bone diseases. Br J Clin Pharmacol 2019;85:1147-60. [PMID: 30357886 DOI: 10.1111/bcp.13803] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
10 Chen W, Li X, Sun L, Sheng W, Huang G. A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects. Mol Genet Genomic Med 2019;7:e847. [PMID: 31297990 DOI: 10.1002/mgg3.847] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]