216 related articles for article (PubMed ID: 1789295)
41. 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]
42. Pallister-Killian syndrome: the first reported case in Hong Kong.
Lo IF; Cheung LY; Lam FW; Lam ST
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(5):333-5. PubMed ID: 9823681
[TBL] [Abstract][Full Text] [Related]
43. [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]
44. 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]
45. Retrospective diagnosis of Pallister-Killian syndrome by CGH array.
Delahaye A; Pipiras E; Delorme-Vincent C; Benkhalifa M; Kasakyan S; Devisme L; Wolf JP; Benzacken B
Fetal Diagn Ther; 2006; 21(6):485-8. PubMed ID: 16969000
[TBL] [Abstract][Full Text] [Related]
46. Skeletal anomalies in a patient with the Pallister/Teschler-Nicola/Killian syndrome.
Kawashima H
Am J Med Genet; 1987 Jun; 27(2):285-9. PubMed ID: 3605214
[TBL] [Abstract][Full Text] [Related]
47. Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p.
Vogel I; Lyngbye T; Nielsen A; Pedersen S; Hertz JM
Am J Med Genet A; 2009 Mar; 149A(3):510-4. PubMed ID: 19215056
[TBL] [Abstract][Full Text] [Related]
48. Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes.
Pauli S; Schmidt T; Funke R; Zoll B; Burfeind P; Dybowski U; Shoukier M; Bartels I
Eur J Med Genet; 2012; 55(8-9):480-4. PubMed ID: 22677035
[TBL] [Abstract][Full Text] [Related]
49. Tetrasomy 12p (Pallister-Killian syndrome): ultrasound indicators and confirmation by interphase fish.
Wilson RD; Harrison K; Clarke LA; Yong SL
Prenat Diagn; 1994 Sep; 14(9):787-92. PubMed ID: 7845885
[TBL] [Abstract][Full Text] [Related]
50. Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosome.
Zhang J; Marynen P; Devriendt K; Fryns JP; Van den Berghe H; Cassiman JJ
Hum Genet; 1989 Nov; 83(4):359-63. PubMed ID: 2807276
[TBL] [Abstract][Full Text] [Related]
51. The Pallister-Killian syndrome is reliably diagnosed by FISH on buccal mucosa.
Manasse BF; Lekgate N; Pfaffenzeller WM; de Ravel TJ
Clin Dysmorphol; 2000 Jul; 9(3):163-5. PubMed ID: 10955474
[TBL] [Abstract][Full Text] [Related]
52. [Pallister-Killian syndrome and 12p tetrasomy: increased LDH-B activity].
Antich Femenias J; Briones Godino MP; Vilaseca Busca MA; Girós Blasco ML; Campos Castelló J; Jaume Roig B; Clusellas Casals N
An Esp Pediatr; 1991 Jun; 34(6):459-62. PubMed ID: 1929015
[No Abstract] [Full Text] [Related]
53. 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]
54. 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]
55. 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]
56. Prenatal diagnosis of Pallister-Killian syndrome.
Soukup S; Neidich K
Am J Med Genet; 1990 Apr; 35(4):526-8. PubMed ID: 1692181
[TBL] [Abstract][Full Text] [Related]
57. Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndrome.
Kaur M; Izumi K; Wilkens AB; Chatfield KC; Spinner NB; Conlin LK; Zhang Z; Krantz ID
PLoS One; 2014; 9(10):e108853. PubMed ID: 25329894
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Prenatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescent in situ hybridization in amniotic fluid cells: a case report of Pallister-Killian syndrome.
Los FJ; Van Opstal D; Schol MP; Gaillard JL; Brandenburg H; Van Den Ouweland AM; in 't Veld PA
Prenat Diagn; 1995 Dec; 15(12):1155-9. PubMed ID: 8750296
[TBL] [Abstract][Full Text] [Related]
60. Interphase fluorescence in situ hybridization analysis of chromosome 12p abnormalities is useful for distinguishing epidermoid cysts of the testis from pure mature teratoma.
Cheng L; Zhang S; MacLennan GT; Poulos CK; Sung MT; Beck SD; Foster RS
Clin Cancer Res; 2006 Oct; 12(19):5668-72. PubMed ID: 17020968
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
