401 related articles for article (PubMed ID: 7897632)
1. 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]
2. 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]
3. 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]
4. 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]
5. Pallister-Killian syndrome in older children and adolescents.
Horneff G; Majewski F; Hildebrand B; Voit T; Lenard HG
Pediatr Neurol; 1993; 9(4):312-5. PubMed ID: 8216546
[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. The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.
Mowery-Rushton PA; Stadler MP; Kochmar SJ; McPherson E; Surti U; Hogge WA
Prenat Diagn; 1997 Mar; 17(3):255-65. PubMed ID: 9110370
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Diaphragmatic hernia in tetrasomy 12p mosaicism.
Bergoffen J; Punnett H; Campbell TJ; Ross AJ; Ruchelli E; Zackai EH
J Pediatr; 1993 Apr; 122(4):603-6. PubMed ID: 8463911
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Pallister-Killian syndrome diagnosed by chorionic villus sampling.
Sharland M; Hill L; Patel R; Patton M
Prenat Diagn; 1991 Jul; 11(7):477-9. PubMed ID: 1754566
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
