Similar articles for PMID: 23169767

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1

Novel clinical manifestations in Pallister-Killian syndrome: comprehensive evaluation of 59 affected individuals and review of previously reported cases.

Wilkens A, Liu H, Park K, Campbell LB, Jackson M, Kostanecka A, Pipan M, Izumi K, Pallister P, Krantz ID. Wilkens A, et al. Am J Med Genet A. 2012 Dec;158A(12):3002-17. doi: 10.1002/ajmg.a.35722. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169767

2

Developmental and behavioral characteristics of individuals with Pallister-Killian syndrome.

Kostanecka A, Close LB, Izumi K, Krantz ID, Pipan M. Kostanecka A, et al. Am J Med Genet A. 2012 Dec;158A(12):3018-25. doi: 10.1002/ajmg.a.35670. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169763

3

Pallister-Killian syndrome: a study of 22 British patients.

Blyth M, Maloney V, Beal S, Collinson M, Huang S, Crolla J, Temple IK, Baralle D. Blyth M, et al. J Med Genet. 2015 Jul;52(7):454-64. doi: 10.1136/jmedgenet-2014-102877. Epub 2015 Apr 17. J Med Genet. 2015. PMID: 25888713

4

Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region.

Izumi K, Conlin LK, Berrodin D, Fincher C, Wilkens A, Haldeman-Englert C, Saitta SC, Zackai EH, Spinner NB, Krantz ID. Izumi K, et al. Am J Med Genet A. 2012 Dec;158A(12):3033-45. doi: 10.1002/ajmg.a.35500. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169682

5

Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome.

Conlin LK, Kaur M, Izumi K, Campbell L, Wilkens A, Clark D, Deardorff MA, Zackai EH, Pallister P, Hakonarson H, Spinner NB, Krantz ID. Conlin LK, et al. Am J Med Genet A. 2012 Dec;158A(12):3046-53. doi: 10.1002/ajmg.a.35726. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169773

6

12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome.

Izumi K, Zhang Z, Kaur M, Krantz ID. Izumi K, et al. Chromosome Res. 2014 Dec;22(4):453-61. doi: 10.1007/s10577-014-9431-y. Epub 2014 Jul 1. Chromosome Res. 2014. PMID: 24981202

7

An Indian boy with additional features in Pallister-Killian syndrome.

Shah K, George R, Balla ES, Oommen SP, Padankatti CS, Srivastava VM, Danda S. Shah K, et al. Indian J Pediatr. 2012 Sep;79(9):1238-40. doi: 10.1007/s12098-011-0585-8. Epub 2011 Oct 20. Indian J Pediatr. 2012. PMID: 22012142

8

Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.

Libotte F, Bizzoco D, Gabrielli I, Mesoraca A, Cignini P, Vitale SG, Marilli I, Gulino FA, Rapisarda AM, Giorlandino C. Libotte F, et al. Taiwan J Obstet Gynecol. 2016 Dec;55(6):863-866. doi: 10.1016/j.tjog.2016.07.010. Taiwan J Obstet Gynecol. 2016. PMID: 28040135 Free article.

9

Postnatal clinical phenotype of five patients with Pallister-Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature.

Alqahtani AS, Putoux A, Bonnet Dupeyron MN, Carneiro M, Lion-Francois L, Rossi M, Tevissen H, Schluth Bolard C, Labalme A, Lesca G, Till M, Edery P, Sanlaville D. Alqahtani AS, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00939. doi: 10.1002/mgg3.939. Epub 2019 Aug 27. Mol Genet Genomic Med. 2019. PMID: 31454185 Free PMC article.

10

Seizure characteristics in Pallister-Killian syndrome.

Candee MS, Carey JC, Krantz ID, Filloux FM. Candee MS, et al. Am J Med Genet A. 2012 Dec;158A(12):3026-32. doi: 10.1002/ajmg.a.35567. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169688

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