396 related articles for article (PubMed ID: 16918638)
1. 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]
2. 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]
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. Tetrasomy 12p--unusual presentation in CVS.
Dong L; Falk RE; Williams J; Kohan M; Schreck RR
Prenat Diagn; 2003 Feb; 23(2):101-3. PubMed ID: 12575013
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21].
Gilgenkrantz S; Fryns JP; Droulle P; Schweitzer M; Chadefaux B; Prieur M
J Genet Hum; 1987 Jan; 35(1):51-61. PubMed ID: 3559524
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
Vermeesch JR; Melotte C; Salden I; Riegel M; Trifnov V; Polityko A; Rumyantseva N; Naumchik I; Starke H; Matthijs G; Schinzel A; Fryns JP; Liehr T
Eur J Med Genet; 2005; 48(3):319-27. PubMed ID: 16179227
[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. 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]
18. 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]
19. 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]
20. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]