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29. Trisomy 4 in a fetus with cyclopia and other anomalies. Van Allen MI; Ritchie S; Toi A; Fong K; Winsor E Am J Med Genet; 1993 Apr; 46(2):193-7. PubMed ID: 8484409 [TBL] [Abstract][Full Text] [Related]
30. Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature. Turan O; Hirfanoğlu IM; Beken S; Biri A; Efetürk T; Atalay Y Turk J Pediatr; 2011; 53(3):337-41. PubMed ID: 21980820 [TBL] [Abstract][Full Text] [Related]
31. Duplication of 9q12-q33: a case report and implications for the dup(9q) syndrome. Stalker HJ; Aymé S; Delneste D; Scarpelli H; Vekemans M; Der Kaloustian VM Am J Med Genet; 1993 Feb; 45(4):456-9. PubMed ID: 8465850 [TBL] [Abstract][Full Text] [Related]
33. Two sibs with partial trisomy 2q. Barnicoat AJ; Abusaad I; Mackie CM; Robards MF Am J Med Genet; 1997 May; 70(2):166-70. PubMed ID: 9128937 [TBL] [Abstract][Full Text] [Related]
34. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example. Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064 [TBL] [Abstract][Full Text] [Related]
35. [Pätau syndrome without trisomy karyotype? Danger of restricted thinking in syndrome diagnosis]. Rode G; Duda V Z Geburtshilfe Perinatol; 1991; 195(3):143-5. PubMed ID: 1926974 [TBL] [Abstract][Full Text] [Related]
36. Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24. Halpern GJ; Shohat M; Merlob P Ann Genet; 1996; 39(3):181-3. PubMed ID: 8839892 [TBL] [Abstract][Full Text] [Related]
37. Trisomy 13/trisomy 18 mosaicism in an infant. Abe K; Harada N; Itoh T; Hirakawa O; Niikawa N Clin Genet; 1996 Nov; 50(5):300-3. PubMed ID: 9007314 [TBL] [Abstract][Full Text] [Related]
38. [Pediatric home care nursing of an infant with trisomy 13 (Patau syndrome)]. Köck-Sauvagerd S Kinderkrankenschwester; 2001 Nov; 20(11):459-61. PubMed ID: 14584130 [No Abstract] [Full Text] [Related]
39. Congenital unilateral absence of orbit with anophthalmos and partial arhinia. Shorey P; Lobo G Indian J Ophthalmol; 1991; 39(3):132-3. PubMed ID: 1841889 [TBL] [Abstract][Full Text] [Related]
40. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly. Ramos-Arroyo MA; de Miguel C; Valiente A; Moreno-Laguna S Am J Med Genet; 1994 Apr; 50(2):177-9. PubMed ID: 8010349 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]