These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 31110634)

  • 1. Pallister-Killian Mosaic Syndrome in an Omani Newborn: A Case Report and Literature Review.
    Elsheikh A; Al Shehhi M; Goud TM; Itoo B; Al Harasi S
    Oman Med J; 2019 May; 34(3):249-253. PubMed ID: 31110634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    Am J Med Genet A; 2012 Dec; 158A(12):3033-45. PubMed ID: 23169682
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00939. PubMed ID: 31454185
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Pallister-Killian syndrome in a child with rare karyotype--a diagnostic problem.
    Smigiel R; Pilch J; Makowska I; Busza H; Slezak R; Sasiadek MM
    Eur J Pediatr; 2008 Sep; 167(9):1063-5. PubMed ID: 18000682
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication.
    Karamysheva TV; Lebedev IN; Minaycheva LI; Nazarenko LP; Kashevarova AA; Fedotov DA; Skryabin NA; Lopatkina ME; Cheremnykh AD; Fonova EA; Nikitina TV; Sazhenova EA; Skleimova MM; Kolesnikov NA; Drozdov GV; Yakovleva YS; Seitova GN; Orishchenko KE; Rubtsov NB
    Front Genet; 2024; 15():1331066. PubMed ID: 38528911
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    J Med Genet; 2015 Jul; 52(7):454-64. PubMed ID: 25888713
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome.
    Lee MN; Lee J; Yu HJ; Lee J; Kim SH
    Ann Lab Med; 2017 Jan; 37(1):66-70. PubMed ID: 27834069
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p.
    Yeung A; Francis D; Giouzeppos O; Amor DJ
    Am J Med Genet A; 2009 Mar; 149A(3):505-9. PubMed ID: 19215037
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome.
    Izumi K; Zhang Z; Kaur M; Krantz ID
    Chromosome Res; 2014 Dec; 22(4):453-61. PubMed ID: 24981202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pallister-Killian syndrome: report of one case.
    Wu HC; Lin LH; Tsai LP; Huang CH; Hung KL; Liao HT
    Acta Paediatr Taiwan; 2006; 47(3):139-41. PubMed ID: 17078467
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.
    Eid MM; Eid OM; Abdel-Hadi S; Hassib N; Madian A; Afifi HH; Abdel-Salam GMH
    J Pediatr Genet; 2020 Sep; 9(3):207-210. PubMed ID: 32714624
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.
    Karaman B; Kayserili H; Ghanbari A; Uyguner ZO; Toksoy G; Altunoglu U; Basaran S
    Mol Cytogenet; 2018; 11():45. PubMed ID: 30140312
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
    Horn D; Majewski F; Hildebrandt B; Körner H
    J Med Genet; 1995 Jan; 32(1):68-71. PubMed ID: 7897632
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype.
    Leube B; Majewski F; Gebauer J; Royer-Pokora B
    Am J Med Genet A; 2003 Dec; 123A(3):296-300. PubMed ID: 14608653
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome.
    Yakut S; Mihci E; Altiok Clark O; Cetin Z; Keser I; Berker S; Luleci G
    Balkan J Med Genet; 2012 Jun; 15(1):61-4. PubMed ID: 24052725
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unclassifiable pattern of hypopigmentation in a patient with mosaic partial 12p tetrasomy without Pallister-Killian syndrome.
    Alesi V; Dentici ML; Restaldi F; Orlando V; Liambo MT; Calacci C; Capolino R; Digilio MC; El Hachem M; Novelli A; Diociaiuti A; Dallapiccola B
    Am J Med Genet A; 2017 Jul; 173(7):1943-1946. PubMed ID: 28489314
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.
    Toydemir RM; Panza E; Longhurst MC; South ST; Rope AF
    Mol Syndromol; 2020 Jul; 11(3):125-129. PubMed ID: 32903844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.
    Theisen A; Rosenfeld JA; Farrell SA; Harris CJ; Wetzel HH; Torchia BA; Bejjani BA; Ballif BC; Shaffer LG
    Am J Med Genet A; 2009 May; 149A(5):914-8. PubMed ID: 19353629
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.