These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Increased fetal nuchal translucency as a sole clue in the prenatal diagnosis of a fetus with trisomy 13. Ki KD; Kim SR; Lee WI Fetal Diagn Ther; 2009; 26(1):54-6. PubMed ID: 19816033 [TBL] [Abstract][Full Text] [Related]
25. Pallister-Killian syndrome: case report with pineal tumor. Mauceri L; Sorge G; Incorpora G; Pavone L Am J Med Genet; 2000 Nov; 95(1):75-8. PubMed ID: 11074499 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosis. Guareschi E; Garavelli L; Pedori S; Di Lernia V; Grenzi L; Franchi F; Marinelli M; Croci GF; Pedretti E; Amarri S; Banchini G; Albertini G Pediatr Dermatol; 2007; 24(4):426-8. PubMed ID: 17845177 [No Abstract] [Full Text] [Related]
28. Abnormal first trimester screen in partial deletion of chromosome 6p21: a case-report. Hulsbergen MH; Van Calenbergh SG; Fryns JP Genet Couns; 2007; 18(2):243-5. PubMed ID: 17710877 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal Abnormalities. Tercanli S; Miny P; Filges I Ultraschall Med; 2015 Oct; 36(5):419-20. PubMed ID: 26759849 [No Abstract] [Full Text] [Related]
33. Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosis. Zollino M; Bajer J; Neri G Prenat Diagn; 1999 Feb; 19(2):184-5. PubMed ID: 10215084 [No Abstract] [Full Text] [Related]
34. A rare abnormal karyotype (45,X/47,XY + 18) associated with increased nuchal translucency thickness. Robertson M; Curren J; Warwick L; Jammu V; Ellwood DA; Dahlstrom JE Ultrasound Obstet Gynecol; 2006 Feb; 27(2):229-31. PubMed ID: 16302283 [No Abstract] [Full Text] [Related]
35. First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoele. Hindryckx A; De Catte L; Van Esch H; Fryns JP; Moerman P; Devlieger R Prenat Diagn; 2008 May; 28(5):445-6. PubMed ID: 18395870 [No Abstract] [Full Text] [Related]
36. Pallister-Killian Syndrome: The Diagnosis is in the Detail. Sailer S; Díaz GA; García MH; Díaz AS; Miguélez JMR; Fernández MEM Klin Padiatr; 2019 Mar; 231(2):93-95. PubMed ID: 30517961 [No Abstract] [Full Text] [Related]
37. The utility of detailed first trimester ultrasound examination in abnormal fetal nuchal translucency. Bronshtein M; Zimmer EZ; Blazer S Prenat Diagn; 2008 Nov; 28(11):1037-41. PubMed ID: 18925580 [TBL] [Abstract][Full Text] [Related]