141 related articles for article (PubMed ID: 1554020)
1. Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome.
Reeser SL; Wenger SL
Am J Med Genet; 1992 Apr; 42(6):815-9. PubMed ID: 1554020
[TBL] [Abstract][Full Text] [Related]
2. Mosaicism in Pallister i(12p) syndrome.
Wenger SL; Boone LY; Steele MW
Am J Med Genet; 1990 Apr; 35(4):523-5. PubMed ID: 2333883
[TBL] [Abstract][Full Text] [Related]
3. New diagnostic method for Pallister-Killian syndrome: detection of i(12p) in interphase nuclei of buccal mucosa by fluorescence in situ hybridization.
Ohashi H; Ishikiriyama S; Fukushima Y
Am J Med Genet; 1993 Jan; 45(1):123-8. PubMed ID: 8418650
[TBL] [Abstract][Full Text] [Related]
4. Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization.
Speleman F; Leroy JG; Van Roy N; De Paepe A; Suijkerbuijk R; Brunner H; Looijenga L; Verschraegen-Spae MR; Orye E
Am J Med Genet; 1991 Dec; 41(3):381-7. PubMed ID: 1789295
[TBL] [Abstract][Full Text] [Related]
5. Cytogenetic study of a severe case of Pallister-Killian syndrome using fluorescence in situ hybridization.
Gamal SM; Hasegawa T; Satoh H; Watanabe T; Endo K; Satoh Y
Jpn J Hum Genet; 1994 Jun; 39(2):259-67. PubMed ID: 8086644
[TBL] [Abstract][Full Text] [Related]
6. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.
Ward BE; Hayden MW; Robinson A
Am J Med Genet; 1988 Dec; 31(4):835-9. PubMed ID: 3239575
[TBL] [Abstract][Full Text] [Related]
7. A case of mosaic tetrasomy 12p (Pallister-Killian Syndrome) diagnosed prenatally: comparison of chromosome analyses of various cells obtained from the patient.
Takakuwa K; Hataya I; Arakawa M; Tamura M; Sekizuka N; Tanaka K
Am J Perinatol; 1997 Nov; 14(10):641-3. PubMed ID: 9605253
[TBL] [Abstract][Full Text] [Related]
8. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
Polityko AD; Goncharova E; Shamgina L; Drozdovskaja N; Podleschuk L; Abramchik E; Jaroshevich E; Khurs O; Pisarik I; Pribushenya O; Rumyantseva N; Naumchik I
J Histochem Cytochem; 2005 Mar; 53(3):361-4. PubMed ID: 15750020
[TBL] [Abstract][Full Text] [Related]
9. Molecular cytogenetic study of patients with Pallister-Killian syndrome.
Larramendy M; Heiskanen M; Wessman M; Ritvanen A; Peltomäki P; Simola K; Kääriäinen H; von Koskull H; Kähkönen M; Knuutila S
Hum Genet; 1993 Mar; 91(2):121-7. PubMed ID: 8462971
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Pallister-Killian syndrome: a mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotype.
Bielanska MM; Khalifa MM; Duncan AM
Am J Med Genet; 1996 Oct; 65(2):104-8. PubMed ID: 8911599
[TBL] [Abstract][Full Text] [Related]
12. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.
Reynolds JF; Daniel A; Kelly TE; Gollin SM; Stephan MJ; Carey J; Adkins WN; Webb MJ; Char F; Jimenez JF
Am J Med Genet; 1987 Jun; 27(2):257-74. PubMed ID: 3605212
[TBL] [Abstract][Full Text] [Related]
13. Pericardial agenesis and focal aplasia cutis in tetrasomy 12p (Pallister-Killian syndrome).
Zakowski MF; Wright Y; Ricci A
Am J Med Genet; 1992 Feb; 42(3):323-5. PubMed ID: 1536171
[TBL] [Abstract][Full Text] [Related]
14. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.
Choo S; Teo SH; Tan M; Yong MH; Ho LY
J Perinatol; 2002; 22(5):420-3. PubMed ID: 12082482
[TBL] [Abstract][Full Text] [Related]
15. Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection.
Schubert R; Viersbach R; Eggermann T; Hansmann M; Schwanitz G
Am J Med Genet; 1997 Oct; 72(1):106-10. PubMed ID: 9295085
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
Raffel LJ; Mohandas T; Rimoin DL
Am J Med Genet; 1986 Aug; 24(4):607-11. PubMed ID: 3740095
[TBL] [Abstract][Full Text] [Related]
17. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
Gerdes AM; Hansen LK; Brandrup F; Soegaard K; Christoffersen A; Rasmussen K
Pediatr Dermatol; 2006; 23(4):378-81. PubMed ID: 16918638
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases.
Warburton D; Anyane-Yeboa K; Francke U
Am J Med Genet; 1987 Jun; 27(2):275-83. PubMed ID: 3605213
[TBL] [Abstract][Full Text] [Related]
20. Lethal Pallister-Killian syndrome: phenotypic similarity with Fryns syndrome.
Rodríguez JI; Garcia I; Alvarez J; Delicado A; Palacios J
Am J Med Genet; 1994 Nov; 53(2):176-81. PubMed ID: 7856644
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
