206 related articles for article (PubMed ID: 18293669)
1. [Pallister-Killian syndrome. Case report].
Ramírez Fernández MA; García Cavazos R; Sánchez Martínez HF
Ginecol Obstet Mex; 2007 Jul; 75(7):412-8. PubMed ID: 18293669
[TBL] [Abstract][Full Text] [Related]
2. Pallister-Killian and Fryns syndromes: nosology.
McPherson EW; Ketterer DM; Salsburey DJ
Am J Med Genet; 1993 Aug; 47(2):241-5. PubMed ID: 8213912
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children).
Mathieu M; Piussan C; Thepot F; Gouget A; Lacombe D; Pedespan JM; Serville F; Fontan D; Ruffie M; Nivelon-Chevallier A; Amblard F; Chauveau P; Moirot H; Chabrolle JP; Croquette MF; Teyssier M; Plauchu H; Pelissier MC; Gilgenkrantz S; Turc-Carel C; Turleau C; Prieur M; Le Merrer M; Gonzales M; Journel H
Ann Genet; 1997; 40(1):45-54. PubMed ID: 9150850
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS.
Bernert J; Bartels I; Gatz G; Hansmann I; Heyat M; Niedmann PD; Rehder H; Waldenmaier C; Zoll B
Am J Med Genet; 1992 Mar; 42(5):747-50. PubMed ID: 1632452
[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. 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]
9. 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]
10. 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]
11. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year].
Chrzanowska K; Fryns JP
J Genet Hum; 1989 Sep; 37(3):259-61. PubMed ID: 2625629
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation.
Frković SH; Durisević IT; Trcić RL; Sarnavka V; Gornik KC; Muzinić D; Letica L; Barić I; Begović D
Coll Antropol; 2010 Mar; 34(1):247-50. PubMed ID: 20437642
[TBL] [Abstract][Full Text] [Related]
16. Late-onset epileptic spasms in children with Pallister-Killian syndrome: a report of two new cases and review of the electroclinical aspects.
Cerminara C; Compagnone E; Bagnolo V; Galasso C; Lo-Castro A; Brinciotti M; Curatolo P
J Child Neurol; 2010 Feb; 25(2):238-45. PubMed ID: 19738236
[TBL] [Abstract][Full Text] [Related]
17. Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported cases.
Struthers JL; Cuthbert CD; Khalifa MM
Am J Med Genet; 1999 May; 84(2):111-5. PubMed ID: 10323734
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]